(30 days)
Not Found
No
The 510(k) summary describes a mechanical guide sheath kit and accessories for bronchoscopy. There is no mention of AI, ML, image processing, or any software-driven analytical capabilities. The performance studies are focused on mechanical and physical properties.
No
The device is described as a kit designed to guide other accessories and/or ultrasonic probes to a target area and collect tissue, specimens, or cells for examination. It does not directly provide therapy.
Yes
The device, specifically its components such as the Single Use Biopsy Forceps and Single Use Cytology Brush, is designed to collect tissue, specimens, or cells for examination (e.g., cytologic examination), which is a key step in diagnosing conditions.
No
The device description clearly outlines physical components such as a guide sheath, biopsy forceps, cytology brush, and stoppers, all of which are sterile and packaged. The performance studies also involve physical testing like radiographic, tensile, dimensional, and trackability testing, indicating a hardware-based device.
Based on the provided text, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- IVD Definition: In Vitro Diagnostics are devices intended for use in the examination of specimens derived from the human body solely or principally for the purpose of providing information concerning a physiological state, state of health, or disease or congenital abnormality. This examination is performed outside of the body (in vitro).
- Device Function: The description clearly states the device is used to guide other instruments within the tracheobronchial tree and collect tissue, specimens, or cells. While these collected samples may be used for in vitro diagnostic testing later, the device itself is a tool for in vivo collection and guidance within the body.
- Lack of Diagnostic Function: The device description and intended use do not mention any analytical or diagnostic function performed by the device itself on the collected samples. It is purely a collection and guidance tool.
Therefore, this device falls under the category of a medical device used for sample collection and procedural guidance, not an In Vitro Diagnostic.
N/A
Intended Use / Indications for Use
Single Use Guide Sheath Kit K-401, K-402
These instruments have been designed to be used with Olympus bronchoscopes, EndoTherapy accessories, and/or ultrasonic probes to guide the EndoTherapy accessories and/or the ultrasonic probes to the target area within the tracheobronchial tree and collect tissue, specimens, or cells bronchoscopically. This kit and its components are intended for adult patients only.
- Indications for use of each component
Single Use Guide Sheath SG-400C
The single use guide sheath has been designed to be used with Olympus bronchoscopes, EndoTherapy accessories, and/or ultrasonic probes to guide the EndoTherapy accessories and/or the ultrasonic probes to the target area within the tracheobronchial tree.
Single Use Biopsy Forceps FB-433D
The biopsy forceps has been designed specifically to collect tissue endoscopically for examination with a flexible bronchoscope within the tracheobronchial tree.
Single Use Cytology Brush BC-205D
The cytology brush has been specifically designed to collect specimens or cells endoscopically for cytologic examination in conjunction with the bronchoscope within the tracheobronchial tree.
Product codes (comma separated list FDA assigned to the subject device)
EOQ, BTG
Device Description
The kit has been designed to be used with Olympus bronchoscopes, EndoTherapy accessories, and/or ultrasonic probes to guide the EndoTherapy accessories and/or the ultrasonic probes to the target area within the tracheobronchial tree and collect tissue, specimens, or cells bronchoscopically.
The compatible bronchoscope for the subject Single Use Guide Sheath Kit needs to have the working length 600mm or less (exclude the ultrasonic bronchoscope) and a working channel inner diameter that is no less than 2.0mm.
The guide sheath kit consists of the following components: Guide Sheath, Biopsy Forceps, with/without Cytology Brush. EU stoppers and US Stopper are also included in the kit as accessories. Each component and the accessory stoppers are sterile and packaged in individual package. All of them are collected into one carton box as one final kit product. Please refer to Table 1 below.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
tracheobronchial tree
Indicated Patient Age Range
adult patients only
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 following performance data are provided in support of the substantial equivalence determination.
No modification was applied to sterilization/shelf-life. Therefore, Sterilization/shelf-life testing was not performed.
No modification was made to the patient contacting materials of the subject device. The modified guide sheath can be covered by the existing biocompatibility testing data provided in the predicate device 510(k).
Performance testing was carried out to demonstrate the safety and the effectiveness of the subject devices. Since the FB-433D and BC-205D have no specification changes, these tests were performed for SG-400C only.
- Radiographic Testing
- Catheter Joint/Tensile Testing
- Dimensional Testing
- Simulated Use Testing
- Trackability Testing (insertion & withdrawal)
Risk analysis for the Single Use Guide Sheath Kit and the Single Use Guiding Device was conducted in accordance with established in-house acceptance criteria based on ISO 14971:2019. The design verification tests and their acceptance criteria were identified and performed as a result of this risk analysis assessment.
Clinical testing was not applicable and not performed.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s): If the device was cleared using the 510(k) pathway, identify the Predicate Device(s) K/DEN number used to claim substantial equivalence and list them here in a comma separated list exactly as they appear in the text. List the primary predicate first in the list.
Reference Device(s): Identify the Reference Device(s) K/DEN number and list them here in a comma separated list exactly as they appear in the text.
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information for the subject device only (e.g. presence / absence, what scope was granted / cleared under the PCCP, any restrictions, etc).
Not Found
§ 874.4680 Bronchoscope (flexible or rigid) and accessories.
(a)
Identification. A bronchoscope (flexible or rigid) and accessories is a tubular endoscopic device with any of a group of accessory devices which attach to the bronchoscope and is intended to examine or treat the larynx and tracheobronchial tree. It is typically used with a fiberoptic light source and carrier to provide illumination. The device is made of materials such as stainless steel or flexible plastic. This generic type of device includes the rigid ventilating bronchoscope, rigid nonventilating bronchoscope, nonrigid bronchoscope, laryngeal-bronchial telescope, flexible foreign body claw, bronchoscope tubing, flexible biopsy forceps, rigid biopsy curette, flexible biopsy brush, rigid biopsy forceps, flexible biopsy curette, and rigid bronchoscope aspirating tube, but excludes the fiberoptic light source and carrier.(b)
Classification. Class II.
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Image /page/0/Picture/0 description: The image contains the logo of the U.S. Food and Drug Administration (FDA). On the left is the Department of Health & Human Services USA seal. To the right of that is the FDA logo, with the letters "FDA" in a blue square. To the right of the square is the text "U.S. FOOD & DRUG ADMINISTRATION" in blue.
Olympus Medical Systems Corp. % Teffany Hutto Regulatory Affairs Consultant Olympus Corporation of the Americas 3500 Corporate Parkway PO Box 610 Center Valley, Pennsylvania 18034-0610
Re: K212667
Trade/Device Name: Single Use Guide Sheath Kit-401, K-402 Regulation Number: 21 CFR 874.4680 Regulation Name: Bronchoscope (Flexible Or Rigid) And Accessories Regulatory Class: Class II Product Code: EOQ, BTG Dated: August 20, 2021 Received: August 23, 2021
Dear Teffany Hutto:
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 may, 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.
1
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 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 (QS) 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 medical devices and radiation-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.
Brandon Blakely, PhD Acting Assistant Director DHT1C: Division of Sleep Disordered Breathing, Respiratory and Anesthesia Devices OHT1: Office of Ophthalmic, Anesthesia, Respiratory, ENT and Dental Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health
Enclosure
2
Indications for Use
510(k) Number (if known)
Device Name Single Use Guide Sheath Kit K-401, K-402
Indications for Use (Describe) Single Use Guide Sheath Kit K-401, K-402
These instruments have been designed to be used with Olympus bronchoscopes, EndoTherapy accessories, and/or ultrasonic probes to guide the EndoTherapy accessories and/or the ultrasonic probes to the target area within the tracheobronchial tree and collect tissue, specimens, or cells bronchoscopically. This kit and its components are intended for adult patients only.
- Indications for use of each component
Single Use Guide Sheath SG-400C
The single use guide sheath has been designed to be used with Olympus bronchoscopes, EndoTherapy accessories, and/or ultrasonic probes to guide the EndoTherapy accessories and/or the ultrasonic probes to the target area within the tracheobronchial tree.
Single Use Biopsy Forceps FB-433D
The biopsy forceps has been designed specifically to collect tissue endoscopically for examination with a flexible bronchoscope within the tracheobronchial tree.
Single Use Cytology Brush BC-205D
The cytology brush has been specifically designed to collect specimens or cells endoscopically for cytologic examination in conjunction with the bronchoscope within the tracheobronchial tree.
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) |
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Image /page/3/Picture/1 description: The image shows the word "OLYMPUS" in large, bold, blue letters. The letters are spaced closely together, and the word is centered in the image. There is a yellow line underneath the word. The registered trademark symbol is located to the right of the letter "S".
Single Use Guide Sheath Kit K-401/K-402
DATE: August 20, 2021
1. General Information
| ■ 510(k) submitter: | OLYMPUS MEDICAL SYSTEMS CORP.
2951 Ishikawa-cho, Hachioji-shi, Tokyo, 192-8507,
Japan
Establishment Registration No: 8010047 |
|-----------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| ■ Contact Person: | Teffany Hutto
Olympus Corporation of the Americas
3500 Corporate Parkway PO Box 610
Center Valley, PA 18034-0610, USA
Phone: 512-508-6550
FAX: 484-896-7128
Email: teffany.hutto@olympus.com |
| ■ Manufacturing site: | Aomori Olympus Co., Ltd.
2-248-1 Okkonoki, Kuroishi-shi, Aomori, 036-0357
Japan
Establishment Registration No.: 9614691 |
2. Device Identification
| ■ Device Trade Name: | Single Use Guide Sheath Kit K-401/K-402
[Component]
- Single Use Guide Sheath SG-400C
- Single Use Biopsy Forceps FB-433D
- Single Use Cytology Brush BC-205D
|
|-------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| | ET Stopper / US Stopper |
| ■ Common Name: | Guide Sheath Kit & Guiding Device |
| ■ Regulation Number: | 874.4680 |
| ■ Regulation Name: | Bronchoscope (flexible or rigid) and accessories |
| ■ Regulatory Class: | II |
| ■ Classification Panel: | Ear Nose & Throat
510(k) Summary
Page 1 of 6 |
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Image /page/4/Picture/0 description: The image shows the word "OLYMPUS" in large, bold, blue letters. The letters are all capitalized and appear to be a sans-serif font. A registered trademark symbol is located to the right of the letter "S".
- Product Code: EOQ , BTG
Predicate Device Information 3.
■ Predicate device
| Device name | 510(k) Submitter | 510(k) No. |
|---|---|---|
| Single Use Guide Sheath Kit K-401/K-402 | OLYMPUS MEDICAL | |
| SYSTEMS CORP. | K192164 |
Device Description 4. Single Use Guide Sheath Kit K-401/K-402
The kit has been designed to be used with Olympus bronchoscopes, EndoTherapy accessories, and/or ultrasonic probes to guide the EndoTherapy accessories and/or the ultrasonic probes to the target area within the tracheobronchial tree and collect tissue, specimens, or cells bronchoscopically.
The compatible bronchoscope for the subject Single Use Guide Sheath Kit needs to have the working length 600mm or less (exclude the ultrasonic bronchoscope) and a working channel inner diameter that is no less than 2.0mm.
The guide sheath kit consists of the following components: Guide Sheath, Biopsy Forceps, with/without Cytology Brush. EU stoppers and US Stopper are also included in the kit as accessories. Each component and the accessory stoppers are sterile and packaged in individual package. All of them are collected into one carton box as one final kit product. Please refer to Table 1 below.
| Components/Accessories in each kit* | ||
|---|---|---|
| Kit Model | K-401 | K-402 |
| Guide Sheath | SG-400C | |
| Biopsy Forceps | FB-433D | |
| Cytology Brush | BC-205D-2010 | NA |
| ET Stopper | ||
| Color: White | Quantity: 4 | Quantity: 3 |
| US Stopper | ||
| Color: Dark gray | Quantity: 1 | Quantity: 1 |
Table 1 Configuration of Each Kit Model and ts/Accossorios in ooch Izit*
The single use guide sheath has been designed to be used with Olympus bronchoscopes, EndoTherapy accessories, and/or ultrasonic probes to guide the EndoTherapy accessories and/or the ultrasonic probes to the target area within the tracheobronchial
5
tree.
This guide sheath is designed to function as an extended working channel. The function of the subject guide sheath is to facilitate obtaining multiple biopsy specimens by leaving the guide sheath in place after localization of the target tissue.
This instrument consists of an insertion portion and a handle portion. The insertion portion is composed of tube and X-ray tip.
The biopsy forceps has been designed specifically to collect tissue endoscopically for examination in conjunction with a flexible bronchoscope. The subject device is allowed to insert into the channel of a bronchoscope with the subject device guide sheath, and then collect tissue with the pair of forceps which is equipped at the distal end of the subject device. Finally, users withdraw the subject device biopsy forceps from the bronchoscope to collect the samples.
The single use cytology brush BC-205D has been designed to collect specimens or cells endoscopically for cytology examination in conjunction with bronchoscopes. The subject device is allowed to insert into the channel of a bronchoscope with the subject device guide sheath, and then collect specimens or cells with the brush which is affixed in the distal end of the subject device. Finally, users withdraw the subject device cytology brush from the bronchoscope to collect the samples.
The ET stopper and US stopper are included in the guide sheath kit as accessory. They are used to fasten the sampling devices (EndoTherapy accessories) or ultrasonic probe to the guide sheath, which serve as a mark to keep the sampling devices or ultrasonic probe in relative position to the guide sheath. The ET stopper are made of silicone rubber outside, molded with stainless steel plate inside.
6
5. Indications for Use
Single Use Guide Sheath Kit K-401, K-402
These instruments have been designed to be used with Olympus bronchoscopes, EndoTherapy accessories, and/or ultrasonic probes to guide the EndoTherapy accessories and/or the ultrasonic probes to the target area within the tracheobronchial tree and collect tissue, specimens, or cells bronchoscopically. This kit and its components are intended for adult patients only.
- Indications for use of each component
Single Use Guide Sheath SG-400C
The single use guide sheath has been designed to be used with Olympus bronchoscopes, EndoTherapy accessories, and/or ultrasonic probes to guide the EndoTherapy accessories and/or the ultrasonic probes to the target area within the tracheobronchial tree.
Single Use Biopsy Forceps FB-433D
The biopsy forceps has been designed specifically to collect tissue endoscopically for examination in conjunction with a flexible bronchoscope within the tracheobronchial tree.
Single Use Cytology Brush BC-205D
The cvtology brush has been specifically designed to collect specimens or cells endoscopically for cytologic examination in conjunction with the bronchoscope within the tracheobronchial tree.
6. Comparison of Technological Characteristics
In comparison to the predicate device, the subject device Single Use Guide Sheath Kit K-401/K-402 have the same technological characteristics as the predicate device except the outer diameter of the SG-400C guide sheath.
The specifications other than outer diameter of the guide sheath are identical to those of the predicate device.
Table 2 Comparison of SG-400C Maximum insertion portion diameter
| SG-400C
(Subject Device) | SG-400C
(Predicate Device :
K192164) |
|-----------------------------|--------------------------------------------|
| φ1.91mm | φ1.95mm |
The difference above has been validated and it is demonstrated that this technological
7
feature does not raise no new safety issues and are substantially equivalent to the predicate device.
The following standards have been applied to the Single Use Guide Sheath Kit.
| Table 3 The list of applicable FDA recognized standards | |
|---|---|
| Standard No. | Standard Title |
| ISO11135 Second Edition | |
| 2014 | Sterilization of Health-Care Products, Ethylene Oxide - |
| Requirements for the Development, Validation and | |
| Routine Control of a Sterilization Process for Medical | |
| Devices | |
| ISO 10993-7 Second | |
| edition 2008-10-15 | Biological evaluation of medical devices - part 7: ethylene |
| oxide sterilization residuals | |
| ISO 11607-1 First edition | |
| 2006-04-15 | Packaging for terminally sterilized medical devices - part |
| 1: requirements for materials, sterile barrier systems and | |
| packaging systems | |
| ISO 11607-2 Second | |
| edition 2019-02 | Packaging for terminally sterilized medical devices - part |
| 2: validation requirements for forming, sealing and | |
| assembly processes | |
| ASTM F1980-16 | Standard Guide For Accelerated Aging Of Sterile Barrier |
| Systems For Medical Devices | |
| ISO 10993-1 Fourth | |
| edition 2009-10-15 | Biological evaluation of medical devices - part 1: |
| evaluation and testing within a risk management process | |
| ISO 10993-5 Third edition | |
| 2009-06-01 | Biological evaluation of medical devices - part 5: tests for |
| in vitro cytotoxicity | |
| ISO 10993-10 Third | |
| Edition 2010-08-01 | Biological evaluation of medical devices - part 10: tests |
| for irritation and skin sensitization | |
| ISO 10993-11 Third | |
| edition 2017-09 | Biological evaluation of medical devices - part 11: tests |
| for systemic toxicity | |
| ISO 14971 Third edition | |
| 2019-12 | Medical devices - application of risk management to |
| medical devices | |
| ASTM F756 | Standard Practice for Assessment of Hemolytic Properties |
| of Materials | |
| ISO 10993-4 Third edition | |
| 2017-04 | Biological evaluation of medical devices - Part 4: |
| Selection of tests for interactions with blood | |
| USP General Chapter |
| Pyrogen Test |
| USP 42, NF 37, General
Chapters | Bacterial Endotoxins Test |
| USP 42, NF 37, General
Chapters | Medical Devices-Bacterial Endotoxin and Pyrogen Tests |
Table 3 The list of applicable FDA recognized standards
8
Image /page/8/Picture/0 description: The image shows the word "OLYMPUS" in large, bold, blue letters. The letters are closely spaced together, creating a solid block of text. A registered trademark symbol is located to the right of the letter "S".
7. Performance Data
The following performance data are provided in support of the substantial equivalence determination.
No modification was applied to sterilization/shelf-life. Therefore, Sterilization/shelf-life testing was not performed.
No modification was made to the patient contacting materials of the subject device. The modified guide sheath can be covered by the existing biocompatibility testing data provided in the predicate device 510(k).
Performance testing was carried out to demonstrate the safety and the effectiveness of the subject devices. Since the FB-433D and BC-205D have no specification changes, these tests were performed for SG-400C only.
- -Radiographic Testing
- Catheter Joint/Tensile Testing -
- Dimensional Testing -
- Simulated Use Testing -
- Trackability Testing (insertion & withdrawal) -
Risk analysis for the Single Use Guide Sheath Kit and the Single Use Guiding Device was conducted in accordance with established in-house acceptance criteria based on ISO 14971:2019. The design verification tests and their acceptance criteria were identified and performed as a result of this risk analysis assessment.
Clinical testing was not applicable and not performed.
8. Conclusion
In comparison to the predicate devices, the Single Use Guide Sheath Kit raises no new safety issues and is substantially equivalent to the predicate device.