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FDA 510(k)

COMEG ENDOSCOPY GRASPING FORCEPS

K-Number: K970489 · 1997-03-19

ApplicantComeg Endoscopy
Decision Date1997-03-19
Product CodeFFL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

COMEG ENDOSCOPY GRASPING FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Comeg Endoscopy. It received FDA 510(k) clearance on 1997-03-19 under 510(k) number K970489. The device is classified under product code FFL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMEG ENDOSCOPY GRASPING FORCEPS?

COMEG ENDOSCOPY GRASPING FORCEPS is a medical device that received FDA 510(k) clearance on 1997-03-19. The listed applicant is Comeg Endoscopy. The 510(k) number is K970489.

When did COMEG ENDOSCOPY GRASPING FORCEPS receive FDA 510(k) clearance?

COMEG ENDOSCOPY GRASPING FORCEPS received FDA 510(k) clearance on 1997-03-19, under 510(k) number K970489.

Who is the listed applicant for COMEG ENDOSCOPY GRASPING FORCEPS?

The FDA 510(k) record lists Comeg Endoscopy as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COMEG ENDOSCOPY GRASPING FORCEPS?

The FDA product code for COMEG ENDOSCOPY GRASPING FORCEPS is FFL.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Comeg Endoscopy as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K971881COMEG RESECTOSCOPE AND LASER-RESECTOSCOPE WORKING ELEMENTS/URETHROTOMES/ELECTRODES/ALBARRAB DEFLECTORSK970764COMEG ENDOSCOPY RESECTOSCOPE ACCESSORIES

Related Devices (Code: FFL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K190492Peralta Stone Removal CatheterCalcula Technologies, Inc.K172299Accordion Piccolo Stone Management DeviceThs International, Inc. D/B/A Accordion MedicalK102887ACCORDION STONE MANAGEMENT DEVICE MODEL AC281205 AND AC3814510Percutaneous Systems, Inc.K082803COAXIAL ACCORDION STONE MANAGEMENT DEVICE, MODEL: COAC12005 - COA20015Percutaneous Systems, Inc.K052048ACCORDIONPercutaneous Systems, IncorporatedK012581REPROCESSED STONE RETRIEVAL BASKETSSterilmed, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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