(73 days)
Not Found
Not Found
No
The 510(k) summary describes a physical medical device (a catheter) and its intended use. There is no mention of software, algorithms, AI, or ML in the description, intended use, or performance studies. The "Mentions AI, DNN, or ML" and "Mentions image processing" fields are explicitly marked as "Not Found".
Yes
The device is a hemodialysis catheter, which is used to treat patients with kidney failure by removing waste products from their blood, thus performing a therapeutic function.
No
Explanation: This device is a chronic hemodialysis catheter, intended for therapeutic procedures like hemodialysis, apheresis, and infusion. There is no mention of it being used to diagnose conditions or diseases.
No
The device description clearly describes a physical catheter made of polyurethane with lumens and extension sets, indicating it is a hardware medical device.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use is for "hemodialysis, apheresis, and infusion." These are procedures performed directly on a patient's body, not on samples taken from the body for diagnostic purposes.
- Device Description: The description details a catheter designed to be inserted into a blood vessel (femoral placement) for direct interaction with the circulatory system. This is characteristic of a therapeutic or procedural device, not a diagnostic one that analyzes samples.
- Lack of IVD Indicators: There is no mention of analyzing biological samples (blood, urine, tissue, etc.), reagents, or any processes related to diagnosing a condition based on in vitro analysis.
IVD devices are specifically designed to examine specimens derived from the human body to provide information for the diagnosis, monitoring, or treatment of a disease or condition. This device's function is to facilitate medical procedures directly within the body.
N/A
Intended Use / Indications for Use
The 14.5 Fr Chronic Hemodialysis Catheter with Symmetrical Tip (Palindrome™) is intended for acute and chronic hemodialysis, apheresis, and infusion. Implantable lengths greater than 40cm are intended for femoral placement.
The 14.5 Fr x 55cm Chronic Hemodialysis Catheter with Symmetrical Tip (Palindrome™) is intended for hemodialysis, apheresis, and infusion, same indications as the predicate device.
The 55cm length is specifically intended for femoral placement.
Product codes
MSD
Device Description
The 14.5 Fr Chronic Hemodialysis Catheter (Palindrome™) has a radiopaque polyurethane shaft with two large inner lumens designed in a "double D" configuration. The distal end of the catheter is designed to a symmetrical tip configuration. The proximal end provides access to two luer lock connection hubs and silicone extension sets.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Not Found
Indicated Patient Age Range
Not Found
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)
Performance data for the femoral length 14.5 Fr Chronic Hemodialysis Catheter with Symmetrical Tip (Results of verification / validation) is included in the test of the predicate device. This new length device is substantially equivalent to the legally marketed device.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
The new length of 14.5 Fr Chronic Hemodialysis Catheter with Symmetrical Tip (Palindrome) is substantially equivalent to the existing sizes of 14.5 Fr Palindrome™ Hemodialysis Catheter in intended use, materials, physical characteristics, and performance characteristics.
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 876.5540 Blood access device and accessories.
(a)
Identification. A blood access device and accessories is a device intended to provide access to a patient's blood for hemodialysis or other chronic uses. When used in hemodialysis, it is part of an artificial kidney system for the treatment of patients with renal failure or toxemic conditions and provides access to a patient's blood for hemodialysis. The device includes implanted blood access devices, nonimplanted blood access devices, and accessories for both the implanted and nonimplanted blood access devices.(1) The implanted blood access device is a prescription device and consists of various flexible or rigid tubes, such as catheters, or cannulae, which are surgically implanted in appropriate blood vessels, may come through the skin, and are intended to remain in the body for 30 days or more. This generic type of device includes various catheters, shunts, and connectors specifically designed to provide access to blood. Examples include single and double lumen catheters with cuff(s), fully subcutaneous port-catheter systems, and A-V shunt cannulae (with vessel tips). The implanted blood access device may also contain coatings or additives which may provide additional functionality to the device.
(2) The nonimplanted blood access device consists of various flexible or rigid tubes, such as catheters, cannulae or hollow needles, which are inserted into appropriate blood vessels or a vascular graft prosthesis (§§ 870.3450 and 870.3460), and are intended to remain in the body for less than 30 days. This generic type of device includes fistula needles, the single needle dialysis set (coaxial flow needle), and the single needle dialysis set (alternating flow needle).
(3) Accessories common to either type include the shunt adaptor, cannula clamp, shunt connector, shunt stabilizer, vessel dilator, disconnect forceps, shunt guard, crimp plier, tube plier, crimp ring, joint ring, fistula adaptor, and declotting tray (including contents).
(b)
Classification. (1) Class II (special controls) for the implanted blood access device. The special controls for this device are:(i) Components of the device that come into human contact must be demonstrated to be biocompatible. Material names and specific designation numbers must be provided.
(ii) Performance data must demonstrate that the device performs as intended under anticipated conditions of use. The following performance characteristics must be tested:
(A) Pressure versus flow rates for both arterial and venous lumens, from the minimum flow rate to the maximum flow rate in 100 milliliter per minute increments, must be established. The fluid and its viscosity used during testing must be stated.
(B) Recirculation rates for both forward and reverse flow configurations must be established, along with the protocol used to perform the assay, which must be provided.
(C) Priming volumes must be established.
(D) Tensile testing of joints and materials must be conducted. The minimum acceptance criteria must be adequate for its intended use.
(E) Air leakage testing and liquid leakage testing must be conducted.
(F) Testing of the repeated clamping of the extensions of the catheter that simulates use over the life of the device must be conducted, and retested for leakage.
(G) Mechanical hemolysis testing must be conducted for new or altered device designs that affect the blood flow pattern.
(H) Chemical tolerance of the device to repeated exposure to commonly used disinfection agents must be established.
(iii) Performance data must demonstrate the sterility of the device.
(iv) Performance data must support the shelf life of the device for continued sterility, package integrity, and functionality over the requested shelf life that must include tensile, repeated clamping, and leakage testing.
(v) Labeling of implanted blood access devices for hemodialysis must include the following:
(A) Labeling must provide arterial and venous pressure versus flow rates, either in tabular or graphical format. The fluid and its viscosity used during testing must be stated.
(B) Labeling must specify the forward and reverse recirculation rates.
(C) Labeling must provide the arterial and venous priming volumes.
(D) Labeling must specify an expiration date.
(E) Labeling must identify any disinfecting agents that cannot be used to clean any components of the device.
(F) Any contraindicated disinfecting agents due to material incompatibility must be identified by printing a warning on the catheter. Alternatively, contraindicated disinfecting agents must be identified by a label affixed to the patient's medical record and with written instructions provided directly to the patient.
(G) Labeling must include a patient implant card.
(H) The labeling must contain comprehensive instructions for the following:
(
1 ) Preparation and insertion of the device, including recommended site of insertion, method of insertion, and a reference on the proper location for tip placement;(
2 ) Proper care and maintenance of the device and device exit site;(
3 ) Removal of the device;(
4 ) Anticoagulation;(
5 ) Management of obstruction and thrombus formation; and(
6 ) Qualifications for clinical providers performing the insertion, maintenance, and removal of the devices.(vi) In addition to Special Controls in paragraphs (b)(1)(i) through (v) of this section, implanted blood access devices that include subcutaneous ports must include the following:
(A) Labeling must include the recommended type of needle for access as well as detailed instructions for care and maintenance of the port, subcutaneous pocket, and skin overlying the port.
(B) Performance testing must include results on repeated use of the ports that simulates use over the intended life of the device.
(C) Clinical performance testing must demonstrate safe and effective use and capture any adverse events observed during clinical use.
(vii) In addition to Special Controls in paragraphs (b)(1)(i) through (v) of this section, implanted blood access devices with coatings or additives must include the following:
(A) A description and material characterization of the coating or additive material, the purpose of the coating or additive, duration of effectiveness, and how and where the coating is applied.
(B) An identification in the labeling of any coatings or additives and a summary of the results of performance testing for any coating or material with special characteristics, such as decreased thrombus formation or antimicrobial properties.
(C) A Warning Statement in the labeling for potential allergic reactions including anaphylaxis if the coating or additive contains known allergens.
(D) Performance data must demonstrate efficacy of the coating or additive and the duration of effectiveness.
(viii) The following must be included for A-V shunt cannulae (with vessel tips):
(A) The device must comply with Special Controls in paragraphs (b)(1)(i) through (v) of this section with the exception of paragraphs (b)(1)(ii)(B), (b)(1)(ii)(C), (b)(1)(v)(B), and (b)(1)(v)(C), which do not apply.
(B) Labeling must include Warning Statements to address the potential for vascular access steal syndrome, arterial stenosis, arterial thrombosis, and hemorrhage including exsanguination given that the device accesses the arterial circulation.
(C) Clinical performance testing must demonstrate safe and effective use and capture any adverse events observed during clinical use.
(2) Class II (performance standards) for the nonimplanted blood access device.
(3) Class II (performance standards) for accessories for both the implanted and the nonimplanted blood access devices not listed in paragraph (b)(4) of this section.
(4) Class I for the cannula clamp, disconnect forceps, crimp plier, tube plier, crimp ring, and joint ring, accessories for both the implanted and nonimplanted blood access device. The devices subject to this paragraph (b)(4) are exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 876.9.
0
.07/914
15 HAMPSHIRE STREET, MANSFIELD, MASSACHUSETTS 02048
510(k) Premarket Notification Palindrome™ 14.5 Fr Chronic Hemodialysis Catheter, Femoral Length
Section B - 510(K) Summary
SEP 2 7 2004
| Date Summary
| Was Prepared: | July 12, 2004 |
|---|---|
| Submitter's | |
| Information: | Kendall |
| a Division of Tyco Healthcare Group LP | |
| 15 Hampshire Street | |
| Mansfield, MA 02048 | |
| Phone: 508-261-8000 | |
| Fax: 508-261-6644 | |
| Contact: | James Welsh |
| Director, Regulatory Affairs | |
| Kendall | |
| a Division of Tyco Healthcare Group LP | |
| Telephone: 508-261-8532 | |
| Fax: 508-261-8461 |
Device Trade
Name: 14.5 Fr Chronic Hemodialysis Catheter with Symmetrical Tip (Palindrome™)
| Device Common | |
|---|---|
| Name: | Catheter, Hemodialysis, Apheresis, Intravascular |
Classification Panel: Gastroenterology
Legally Marketed Devices To Which Substantial Equivalence Is Claimed:
The new length of 14.5 Fr Chronic Hemodialysis Catheter with Symmetrical Tip (Palindrome) is substantially equivalent to the existing sizes of 14.5 Fr Palindrome™ Hemodialysis Catheter in intended use, materials, physical characteristics, and performance characteristics. The modifications attributed to the predicate device are a longer shaft length, and an indication for placing the catheter via the femoral vein.
1
KOH 1914 Page 20
KENDALL 15 HAMPSHIRE STREET, MANSFIELD, MASSACHUSET $ 02048 . (508) 261-8000
510(k) Premarket Notification Palindrome™ 14.5 Fr Chronic Hemodialysis Catheter, Femoral Length Section B - 510(K) Summary
Device Description:
The 14.5 Fr Chronic Hemodialysis Catheter (Palindrome™) has a radiopaque The 14:3 FT Chronic Hemodiaryold Oatholor (Fullinens designed in a "double D" configuration. polyurethane shalt with two large inner lantens doetigal tip configuration. The proximal The distal end of the batheter oxlorido to a official to a synimaly and silicone extension sets.
Intended Use:
The 14.5 Fr Chronic Hemodialysis Catheter with Symmetrical Tip (Palindrome™) is The 14.5 I I Onfonio Fiemodialysis, apheresis, and infusion. It may be intended for actic and onlynie nemonation in mplantable lengths greater than 40cm are intended for femoral placement
Performance Data: Performance data for the femoral length 14.5 Fr Chronic Performance Data: Performance data for the lemoral lorgen in the least of the Herriodialysis Oatheter with Cyminooloal Tip (Results of verification / validation predicate device laontined ingth device is substantially equivalent to the legally marketed device.
2
Image /page/2/Picture/1 description: The image shows the logo for the Department of Health & Human Services - USA. The logo consists of a circle with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged around the circumference. Inside the circle is a stylized image of an eagle.
SEP 2 7 2004
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
Mr. James Welsh Director, Regulatory Affairs Kendall A Division of Tyco Healthcare Group LP 15 Hampshire Street MANSFIELD MA 02048
Re: K041914
Trade/Device Name: Palindrome™ 14.5Fr 55cm Chronic Hemodialysis Catheter Regulation Number: 21 CFR §876.5540 Regulation Name: Blood access device and accessories Regulatory Class: III Product Code: 78 MSD Dated: July 12, 2004 Received: July 16, 2004
Dear Mr. Welsh:
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). You may, therefore, market the device, subject to the general controls provisions of the Act. However, you are responsible to determine that the medical devices you use as components in the kit have either been determined as substantially equivalent under the premarket notification process (Section 510(k) of the act), or were legally on the market prior to May 28, 1976, the enactment date of the Medical Device Amendments. Please note: If you purchase your device components in bulk (i.e., unfinished) and further process (e.g., sterilize) you must submit a new 510(k) before including these components in your kit. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, and labeling, and prohibitions against misbranding and adulteration.
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.
3
Page 2 - Mr. James Welsh
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 requirements, including, but not limited to: registration (21 CFR Part 807); listing (21 CFR Part 807), labeling (21 CFR Part 801); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
This letter will allow you to begin marketing your device as described in your Section 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market. If you desire specific advice for your device on the labeling regulation, please contact the Office of Compliance at (301) 594-4616. Also, please note the regulation entitled, "Misbranding by reference to premarket notification"(21 CFR Part 807.97). You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll free number (800) 638-2041 or (301) 443-6597, or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html.
Sincerely yours,
David h. Segerson
for
N
E
Nancy C. Brogdon Director, Division of Reproductive, Abdominal, and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
4
K041917
2048 • (508) 261-8000
15 HAMPSHIRE STREET, MANSFIELD, MASSACHUSETTS 020
510(k) Premarket Notification 510(k) Premarket Notification
Palindrome™ 14.5 Fr Chronic Hemodialysis Catheter, Femoral Length
Appendix 1
Indications for Use Statement
Device Name:
Bevios Names
14.5 Fr x 55cm Chronic Hemodialysis Catheter with Symmetrical Tip (Palindrome™)
14.5 Fr x 55cm Chronic Hemodialysis Catheter with Symmetrical Tip (Palindrome™)
Indications for Use:
multations for of Som Chronic Hemodialysis Catheter with Symmetrical Tip (Palindrome)") is
The 14.5 Fr x didenia, anbergesis, and infusion, same indications as the predica The 14.5 Fr x 55cm Chronic Hemodialysis Cathere with Syrimlerical The 14.5 Fr x
intended for hemodialysis Catheresis, and infusions as the predicate device.
The state the sec intended for hemodialysis, aprerests, and infaorial of a
The 55cm length is specifically intended for femoral placement.
Please Do Not Write Below This Line – Continue On Another Page If Needed
Concurrence of CDRH, Office of Device Evaluation (ODE)
Prescription Use_ X (Per 21 CFR 801 109) OR
Over-The-Counter Use_
Daniel A. Seymann
(Division Sign-Off) (Division Sign-Oil)
Division of Reproductive, Abdominal, Division of Radiological Devic 510(k) Number