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FDA 510(k)

FORCEPS, GRASPING, FLEXIBLE ENDOSCOPIC

K-Number: K954377 · 1995-10-26

ApplicantAnnex Medical, Inc.
Decision Date1995-10-26
Product CodeFFL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FORCEPS, GRASPING, FLEXIBLE ENDOSCOPIC is the device name listed in this FDA 510(k) record. The listed applicant is Annex Medical, Inc.. It received FDA 510(k) clearance on 1995-10-26 under 510(k) number K954377. 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 FORCEPS, GRASPING, FLEXIBLE ENDOSCOPIC?

FORCEPS, GRASPING, FLEXIBLE ENDOSCOPIC is a medical device that received FDA 510(k) clearance on 1995-10-26. The listed applicant is Annex Medical, Inc.. The 510(k) number is K954377.

When did FORCEPS, GRASPING, FLEXIBLE ENDOSCOPIC receive FDA 510(k) clearance?

FORCEPS, GRASPING, FLEXIBLE ENDOSCOPIC received FDA 510(k) clearance on 1995-10-26, under 510(k) number K954377.

Who is the listed applicant for FORCEPS, GRASPING, FLEXIBLE ENDOSCOPIC?

The FDA 510(k) record lists Annex Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FORCEPS, GRASPING, FLEXIBLE ENDOSCOPIC?

The FDA product code for FORCEPS, GRASPING, FLEXIBLE ENDOSCOPIC is FFL.

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Other records listing Annex Medical, Inc. 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.

K951532METAL URETERAL BASKET STONE DISLODGERK952863FORCEPS, BIOPSY, NON-ELECTRICK951761METEL URETERAL BASKET STONE DISLODGERK934636ANNEX MEDICAL FLAT WIRE STONE EXTRACTORK934675METAL URETERAL BASKET STONE DISLODGERK934598GRASPING FORCEPS OR RETRIEVAL FORCEPS

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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

View on FDA Database →

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

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