(200 days)
No
The description focuses on the physical components, materials, and performance characteristics of a standard enteral feeding catheter and stylet. There is no mention of any software, algorithms, or data processing that would indicate the use of AI or ML.
Yes.
Explanation: The device is an enteral feeding catheter used for providing nutrition, which classifies it as a therapeutic device.
No
Explanation: The device description and intended use clearly state that this is an enteral feeding catheter, used for delivering tube feedings. There is no mention of it being used to diagnose conditions or gather physiological information for diagnostic purposes.
No
The device description explicitly details physical components like a catheter, stylet, connectors, and materials (polyurethane, stainless steel, polycarbonate), indicating it is a hardware medical device.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- IVD Definition: In Vitro Diagnostic devices are used to examine specimens taken from the human body (like blood, urine, or tissue) to provide information for diagnosis, monitoring, or screening.
- Device Function: The Enteral Feeding Catheter is a medical device used to deliver nutrition directly into the stomach or intestines. It is a physical device inserted into the body for therapeutic purposes (feeding), not for analyzing biological samples.
- Intended Use: The intended use clearly states it's for "intermittent or continuous tube feedings." This is a direct intervention, not a diagnostic test.
- Device Description: The description details the physical components and materials of a catheter designed for insertion and delivery of substances.
- Performance Studies: The performance studies focus on the physical and biological compatibility of the device itself (biocompatibility, bench testing), not on the accuracy or reliability of a diagnostic test.
Therefore, the Enteral Feeding Catheter falls under the category of a therapeutic medical device, not an In Vitro Diagnostic device.
N/A
Intended Use / Indications for Use
Enteral feeding catheter is intended for use in those patients who require intermittent or continuous tube feedings via the nasogastric or nasoenteric route. The target population is adults and pediatrics.
Product codes
KNT
Device Description
The Enteral Feeding Catheter is composed of a feeding catheter and stylet and can be divided into Funnel type and Enfit type as per the structure of the feeding catheter. For Funnel type, the feeding catheter is composed of tip, body, Y connector. The Y connector has integrated protective cap and strap. For Enfit type, the feeding catheter is composed of tip, body, Y connector, protective cap, and strap. The feeding catheter is made of polyurethane tube with BNF-II-79 hydrophilic coating. The feeding catheter is available in sizes of 6Fr, 8Fr, 10Fr and lengths of 70cm, 100cm, 120cm and 140cm. The length is measured from the distal tip to the proximal hub. The distal end of the feeding catheter features a sideport and is a smooth rounded finish. The proximal end of the feeding catheter features a funnel Y connector that is made of polyurethane or Enfit Y connector that is made of polycarbonate. A stainless-steel stylet with a length corresponding to the feeding catheter is fit inside the feeding catheter.
The subject device, Enteral Feeding Catheter, may be introduced directly when there is adequate peristalsis and no gastric outlet obstruction. Alternatively, the feeding catheter may be passed over a stylet. The feeding catheter is intended to be indwelling up to four weeks and is for single-use only.
The Enteral Feeding Catheter has model numbers of EF4064M, EF4084M, EF4084H, EF4104M, EF4104L, EF4124L, EF4124X, EF4065M, EF4085M, EF4085H, EF4105M, EF4105L, EF4125L and EF4125X.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
nasogastric or nasoenteric route (for placement, leading to stomach, duodenum or jejunum)
Indicated Patient Age Range
adults and pediatrics
Intended User / Care Setting
Not Found
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
Not Found
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
The subject device, Enteral Feeding Catheter, was subjected to biocompatibility testing and bench testing (Zero Time and Accelerated Aged).
Biocompatibility Testing:
- In vitro cytotoxicity, per ISO 10993-5: 2009.
- Implantation, per ISO 10993-6: 2016.
- Intracutaneous reactivity, per ISO 10993-10: 2010.
- Skin sensitization, per ISO 10993-10: 2010.
- Acute systemic toxicity, per ISO 10993-11: 2017.
- Subacute toxicity, per ISO 10993-11: 2017.
- Pyrogenicity, per ISO 10993-11: 2017 and USP General Chapter .
Bench Testing (Zero Time and Accelerated Aged): - Appearance, per similar device and product characteristics.
- Dimensions, per similar device and product characteristics.
- Tensile property, per EN 1615: 2000.
- Connector compatibility, per EN 1615: 2000.
- Connector tensile property, per EN 1615: 2000.
- Liquid leakage, per EN 1615: 2000.
- Flow rate, per EN 1618: 1997.
- Acid assistance, per product characteristics.
- Coating lubricity, per product characteristics.
- Radio-detectability, per similar device and product characteristics.
- Stylet tensile force, per EN 1618: 1997.
- Style corrosion, per ISO 11070: 2014.
- Style fracture test, per ISO 11070: 2014.
- Chemical performance, per ISO 8536-4: 2019.
- Sterility, per EN 1615: 2000 and ISO 11135: 2014.
- Bacterial endotoxin, per ANSI/AAMI ST72: 2011.
- Package performance, per ISO 11607-1: 2019 and ISO 11607-2: 2019.
- Shelf Life Validation, per ASTM F1980-16.
Key results: The results of these tests confirm that the Enteral Feeding Catheter meets the design input requirements based on the intended use and support the conclusion that this device does not raise new questions of safety and/or effectiveness and is substantially equivalent to the predicate device.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
Reference Device(s)
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 876.5980 Gastrointestinal tube and accessories.
(a)
Identification. A gastrointestinal tube and accessories is a device that consists of flexible or semi-rigid tubing used for instilling fluids into, withdrawing fluids from, splinting, or suppressing bleeding of the alimentary tract. This device may incorporate an integral inflatable balloon for retention or hemostasis. This generic type of device includes the hemostatic bag, irrigation and aspiration catheter (gastric, colonic, etc.), rectal catheter, sterile infant gavage set, gastrointestinal string and tubes to locate internal bleeding, double lumen tube for intestinal decompression or intubation, feeding tube, gastroenterostomy tube, Levine tube, nasogastric tube, single lumen tube with mercury weight balloon for intestinal intubation or decompression, and gastro-urological irrigation tray (for gastrological use).(b)
Classification. (1) Class II (special controls). The barium enema retention catheter and tip with or without a bag that is a gastrointestinal tube and accessory or a gastronomy tube holder accessory is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 876.9.(2) Class I (general controls) for the dissolvable nasogastric feed tube guide for the nasogastric tube. The class I device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to § 876.9.
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Image /page/0/Picture/0 description: The image contains the logo of the U.S. Food and Drug Administration (FDA). The logo consists of two parts: the Department of Health & Human Services USA seal on the left and the FDA acronym followed by the full name of the agency, "U.S. Food & Drug Administration," on the right. The FDA part of the logo is in blue, with the acronym in a solid blue square and the agency's name in a lighter shade of blue.
April 9, 2021
Medcaptain Life Science Co., Ltd. Mr. David Xia 601, Building C, Jinweiyuan Industrial Park, Pingshan District Shenzhen, Guangdong 518118 CHINA
K202748 Re:
Trade/Device Name: Enteral Feeding Catheter Regulation Number: 21 CFR 876.5980 Regulation Name: Gastrointestinal Tube and accessories Regulatory Class: Class II Product Code: KNT Dated: February 2, 2021 Received: February 8, 2021
Dear David Xia:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You mav. therefore, market the device, subject to the general controls provisions of the Act. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database located at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's
1
requirements, including, but not limited to: registration and listing (21 CFR Part 807): labeling (21 CFR Part 801); medical device reporting of medical device-related adverse events) (21 CFR 803) for devices or postmarketing safety reporting (21 CFR 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reportingcombination-products); good manufacturing practice requirements as set forth in the quality systems (0S) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems.
For comprehensive regulatory information about mediation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medicaldevices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-device-advice-comprehensive-regulatoryassistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100).
Sincerely,
Yasaman Z. Ardeshirpour -S
for
Shanil P. Haugen, Ph.D. Assistant Director DHT3A: Division of Renal, Gastrointestinal, Obesity and Transplant Devices OHT3: Office of GastroRenal, ObGyn, General Hospital and Urology Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health
Enclosure
2
DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration
Indications for Use
Form Approved: OMB No. 0910-0120 Expiration Date: 06/30/2020 See PRA Statement below.
510(k) Number (if known) K202748
Device Name
Enteral Feeding Catheter.
Indications for Use (Describe)
Enteral feeding catheter is intended for use in those patients who require intermittent or continuous tube feedings via the nasogastric or nasoenteric route. The target population is adults and pediatrics.
Type of Use (Select one or both, as applicable)
Prescription Use (Part 21 CFR 801 Subpart D)
Over-The-Counter Use (21 CFR 801 Subpart C)
CONTINUE ON A SEPARATE PAGE IF NEEDED.
This section applies only to requirements of the Paperwork Reduction Act of 1995,
*DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW."
The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to:
Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff@fda.hhs.gov
"An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number."
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Image /page/3/Picture/0 description: The image shows the logo for MEDCAPTAIN. The text "MEDCAPTAIN" is in a sans-serif font, with "MED" in gray and "CAPTAIN" in blue. To the right of the text is a stylized speech bubble in blue and orange. Above the text is the company name in Chinese characters.
MEDCAPTAIN LIFE SCIENCE CO., LTD. 601Building C, Jinweiyuan Industrial Park, Pingshan District, Shenzhen, Guangdong, CN 518118. Tel .: +86-755-28380626 Email: disposable@medcaptain.com Fax .: +86-755-84517910 Website: www.medcaptain.com
510(k) Summary
I. Submitter/510(k) Holder
| Submission: | Traditional 510(k) Premarket Notification |
|---|---|
| Submitter: | MEDCAPTAIN LIFE SCIENCE CO., LTD. |
| Address: | 601, Building C, Jinweiyuan Industrial Park, Pingshan |
| District, Shenzhen, Guangdong, CN 518118. | |
| Contact Person: | David Xia |
| Telephone: | +86-755-28380626 |
| Telefax: | +86-755-84517910 |
| Email: | david.xia@medcaptain.com |
| Date prepared: | April 9, 2021 |
II. Device
| Device Trade Name: | Enteral Feeding Catheter |
|---|---|
| Device Common Name: | Feeding Tube or NG/NI Tube |
| Regulatory Name: | Gastrointestinal Tube and Accessories |
| Regulation Number: | 21 CFR 876.5980 |
| Product Code: | KNT |
| Product Code Name: | Tubes, Gastrointestinal (And Accessories) |
| Regulatory Class: | Class II |
| Device Panel: | Gastroenterology and Urology |
III. Predicate Device and reference device
The Enteral Feeding Catheter is substantially equivalent to the following device: Corpark Enteric Feeding Tube W/Guide Tip (K821906, CORPARK MEDSYSTEMS) cleared on December 29, 2008.
| 510(k) submitter/holder: | CORPAK MEDSYSTEMS |
|---|---|
| 510(k) number: | K821906 |
| Device Trade Name: | Corpark Enteric Feeding Tube W/Guide Tip |
| Regulatory Name: | Gastrointestinal Tube and Accessories |
| Regulation Number: | 21 CFR 876.5980 |
| Product Code: | KNT |
| Product Code Name: | Tubes, Gastrointestinal (And Accessories) |
| Regulatory Class: | Class II |
| Device Panel: | Gastroenterology and Urology |
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Image /page/4/Picture/0 description: The image contains the logo for MEDCAPTAIN. The text "MEDCAPTAIN" is written in a combination of gray and blue colors. To the right of the text, there is an orange bracket symbol. Above the MEDCAPTAIN logo, there are three Chinese characters written in gray.
IEDCAPTAIN LIFE SCIENCE CO., LTD. 601Building C, Jinweiyuan Industrial Park, Pingshan District, Shenzhen, Guangdong, CN 518118. Tel .: +86-755-28380626 Email: disposable@medcaptain.com Fax .: +86-755-84517910 Website: www.medcaptain.com
The reference device, Cediflo Enteral Feeding Tubes & Cediflo Junior Enteral Feeding Tubes (K181787, Cedic S.R.L.) was used in this submission.
| 510(k) submitter/holder: | Cedic S.R.L. |
|---|---|
| 510(k) number: | K181787 |
| Device Trade Name: | Cediflo Enteral Feeding Tubes & Cediflo Junior |
| Enteral Feeding Tubes | |
| Regulatory Name: | Gastrointestinal Tubes With Enteral Specific |
| Connectors | |
| Regulation Number: | 21 CFR 876.5980 |
| Product Code: | PIF |
| Product Code Name: | Gastrointestinal Tubes With Enteral Specific |
| Connectors | |
| Regulatory Class: | Class II |
| Device Panel: | Gastroenterology and Urology |
IV. Device Description
The Enteral Feeding Catheter is composed of a feeding catheter and stylet and can be divided into Funnel type and Enfit type as per the structure of the feeding catheter. For Funnel type, the feeding catheter is composed of tip, body, Y connector. The Y connector has integrated protective cap and strap. For Enfit type, the feeding catheter is composed of tip, body, Y connector, protective cap, and strap. The feeding catheter is made of polyurethane tube with BNF-II-79 hydrophilic coating. The feeding catheter is available in sizes of 6Fr, 8Fr, 10Fr and lengths of 70cm, 100cm, 120cm and 140cm. The length is measured from the distal tip to the proximal hub. The distal end of the feeding catheter features a sideport and is a smooth rounded finish. The proximal end of the feeding catheter features a funnel Y connector that is made of polyurethane or Enfit Y connector that is made of polycarbonate. A stainless-steel stylet with a length corresponding to the feeding catheter is fit inside the feeding catheter.
The subject device, Enteral Feeding Catheter, may be introduced directly when there is adequate peristalsis and no gastric outlet obstruction. Alternatively, the feeding catheter may be passed over a stylet. The feeding catheter is intended to be indwelling up to four weeks and is for single-use only.
The Enteral Feeding Catheter has model numbers of EF4064M, EF4084M, EF4084H, EF4104M, EF4104L, EF4124L, EF4124X, EF4065M, EF4085M, EF4085H, EF4105M, EF4105L, EF4125L and EF4125X. The differences of each model are listed in the following table 1.
Table 1 Models of Enteral feeding catheter
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Image /page/5/Picture/0 description: The image shows the logo for MEDCAPTAIN. The text "MEDCAPTAIN" is written in a combination of gray and blue letters, with the last part of the word in blue and enclosed in a bracket-like shape. Above the word "MEDCAPTAIN" are two Chinese characters in gray.
MEDCAPTAIN LIFE SCIENCE CO., LTD. 601Building C, Jinweiyuan Industrial Park, Pingshan District, henzhen. Guangdong. CN 518118. Email: disposable@medcaptain.com Tel .: +86-755-28380626 Fax .: +86-755-84517910 Website: www.medcaptain.com
| Enteral feeding catheter | |||||
|---|---|---|---|---|---|
| Models | Feeding catheter | Stylet | |||
| Type | Size | Effective length(cm) | Effective length(cm) | Color of hub | |
| EF4064M | Funnel | 6Fr | 70 | 70 | Green |
| EF4084M | Funnel | 8Fr | 70 | 70 | Blue |
| EF4084H | Funnel | 8Fr | 100 | 100 | Blue |
| EF4104M | Funnel | 10Fr | 70 | 70 | Black |
| EF4104L | Funnel | 10Fr | 120 | 120 | Black |
| EF4124L | Funnel | 12Fr | 120 | 120 | White |
| EF4124X | Funnel | 12Fr | 140 | 140 | White |
| EF4065M | Enfit | 6Fr | 70 | 70 | Green |
| EF4085M | Enfit | 8Fr | 70 | 70 | Blue |
| EF4085H | Enfit | 8Fr | 100 | 100 | Blue |
| EF4105M | Enfit | 10Fr | 70 | 70 | Black |
| EF4105L | Enfit | 10Fr | 120 | 120 | Black |
| EF4125L | Enfit | 12Fr | 120 | 120 | White |
| EF4125X | Enfit | 12Fr | 140 | 140 | White |
V. Indications for Use
Enteral Feeding Catheter is intended for use in those patients who require intermittent or continuous tube feedings via the nasogastric or nasoenteric route. The target population is adults and pediatrics.
VI. Comparison of Technological Characteristics with the Predicate Device
The subject device, Enteral Feeding Catheter, and the predicate device, Corpark Enteric Feeding Tube W/Guide Tip, are substantially equivalent in that these devices have similar intended use, technological characteristics, target user, patient population, placement location, use environment, etc. The subject device and predicate device similarly establish an enteral delivery for feeding. The subject device and predicate device have identical characteristics including the number of side port on the distal end of the catheter and rounded distal tip, tube material and tube type. The subject device and predicate device are inserted into stomach, duodenum or jejunum of the patient via the nasogastric or nasoenteric route.
The differences between the subject and the predicate device include the materials of coating, tube size and length, sterilization, energy type and shelf life. The materials Page 3 of 5
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Image /page/6/Picture/0 description: The image shows the logo for MEDCAPTAIN. The text "MEDCAPTAIN" is in blue and gray, with the "CAPTAIN" portion in blue. To the right of the text is a stylized orange bracket. Above the text is a logo in gray, which appears to be Chinese characters.
MEDCAPTAIN LIFE SCIENCE CO., LTD. 601Building C, Jinweiyuan Industrial Park, Pingshan District, Shenzhen, Guangdong, CN 518118. Tel .: +86-755-28380626 Email: disposable@medcaptain.com Fax .: +86-755-84517910 Website: www.medcaptain.com
of subject device are biocompatible based on biocompatibility tests. The tube size and length of the subject device is covered by those of the predicate device. Sterilization process has been proved to be qualified and can keep SAL=10c. The sterility and energy type of the subject device is addressed from a technological perspective by the reference device, Cediflo Enteral Feeding Tubes. The shelf life has been proved that the technical performance of the device will be qualified within 3 years. All these differences do not raise any new issues of safety and/or effectiveness.
VII. Performance Data
The subject device, Enteral Feeding Catheter, was subjected to the following applicable testing to assure reliable design and performance under the specified testing parameters:
Biocompatibility Testing:
Per ISO 10993-1: 2018 and FDA guidance, the following tests were performed to ensure the biocompatibility of the subject device.
- In vitro cytotoxicity, per ISO 10993-5: 2009 .
- Implantation, per ISO 10993-6: 2016 ●
- Intracutaneous reactivity, per ISO 10993-10: 2010 ●
- Skin sensitization, per ISO 10993-10: 2010 .
- Acute systemic toxicity, per ISO 10993-11: 2017 .
- Subacute toxicity, per ISO 10993-11: 2017 .
- Pyrogenicity, per ISO 10993-11: 2017 and USP General Chapter .
Bench Testing (Zero Time and Accelerated Aged):
Per EN 1615: 2000, EN 1618: 1997, ISO 80369-3: 2016, etc., the following tests were performed to ensure performance/functionality of the subject device.
- Appearance, per similar device and product characteristics. .
- Dimensions, per similar device and product characteristics.
- . Tensile property, per EN 1615: 2000.
- Connector compatibility, per EN 1615: 2000. .
- Connector tensile property, per EN 1615: 2000. .
- . Liquid leakage, per EN 1615: 2000.
- Flow rate, per EN 1618: 1997. .
- Acid assistance, per product characteristics. ●
- . Coating lubricity, per product characteristics.
- Radio-detectability, per similar device and product characteristics. .
- Stylet tensile force, per EN 1618: 1997. .
- Style corrosion, per ISO 11070: 2014. .
- Style fracture test, per ISO 11070: 2014. .
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Image /page/7/Picture/0 description: The image shows the logo for MEDCAPTAIN. The word "MED" is in gray, and the word "CAPTAIN" is in blue. To the right of the word "CAPTAIN" is an orange bracket. Above the word "MEDCAPTAIN" are three Chinese characters in gray.
MEDCAPTAIN LIFE SCIENCE CO., LTD. 601Building C, Jinweiyuan Industrial Park, Pingshan District, Shenzhen, Guangdong, CN 518118. Tel .: +86-755-28380626 Email: disposable@medcaptain.com Fax .: +86-755-84517910 Website: www.medcaptain.com
- Chemical performance, per ISO 8536-4: 2019. .
- . Sterility, per EN 1615: 2000 and ISO 11135: 2014.
- Bacterial endotoxin, per ANSI/AAMI ST72: 2011. .
- Package performance, per ISO 11607-1: 2019 and ISO 11607-2: 2019. .
- Shelf Life Validation, per ASTM F1980-16. .
Clinical Tests:
Clinical tests were not required to demonstrate of Enteral feeding catheter. Product functionality has been adequately assessed by non-clinical tests.
Animal Tests:
Animal tests were not required to demonstrate performance of Enteral feeding catheter. Product functionality has been adequately assessed by non-animal tests.
VIII. Conclusions
The results of these tests confirm that the Enteral Feeding Catheter meets the design input requirements based on the intended use and support the conclusion that this device does not raise new questions of safety and/or effectiveness and is substantially equivalent to the predicate device, Corpark Enteric Feeding Tube W/Guide Tip (K821906, CORPARK MEDSYSTEMS).