FDA 510(k)

GRASPING FORCEPS, BIOPSY FORCEPS, SPOON FORCEPS

K-Number: K935070 · 1994-01-25

ApplicantKARL STORZ Endoscopy-America, Inc.

Decision Date1994-01-25

Product CodeFCL

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

GRASPING FORCEPS, BIOPSY FORCEPS, SPOON FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is KARL STORZ Endoscopy-America, Inc.. It received FDA 510(k) clearance on 1994-01-25 under 510(k) number K935070. The device is classified under product code FCL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRASPING FORCEPS, BIOPSY FORCEPS, SPOON FORCEPS?

GRASPING FORCEPS, BIOPSY FORCEPS, SPOON FORCEPS is a medical device that received FDA 510(k) clearance on 1994-01-25. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K935070.

When did GRASPING FORCEPS, BIOPSY FORCEPS, SPOON FORCEPS receive FDA 510(k) clearance?

GRASPING FORCEPS, BIOPSY FORCEPS, SPOON FORCEPS received FDA 510(k) clearance on 1994-01-25, under 510(k) number K935070.

Who is the listed applicant for GRASPING FORCEPS, BIOPSY FORCEPS, SPOON FORCEPS?

The FDA 510(k) record lists KARL STORZ Endoscopy-America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GRASPING FORCEPS, BIOPSY FORCEPS, SPOON FORCEPS?

The FDA product code for GRASPING FORCEPS, BIOPSY FORCEPS, SPOON FORCEPS is FCL.

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Other records listing KARL STORZ Endoscopy-America, Inc. as applicant

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Related Devices (Code: FCL)

K032092OLYMPUS XCYF-TP3 CYSTOFIBERSCOPE/NEPHROFIBERSCOPEOlympus Optical Co., Ltd.K973611SPECTRASCIENCE REUSABLE BIOPSY FORCEPSSpectrascience, Inc.K971315AUXILIARY INSTRUMENTS FOR URSRichard Wolf Medical Instruments Corp.K964120INJECTO FLUSHRobert J. Jynch, Jr.K963517SPECTRA SCIENCE BIOPSY FORCEPSSpectrascience, Inc.K955065OLYMPUS FB SERIES BIOPSY FORCEPSOlympus America, 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.