FDA 510(k)

MINI FORCEPS WITH HF, 3.5MM; MICRO FORCEPS WITH HF, 2MM

K-Number: K973648 · 1997-12-17

ApplicantRichard Wolf Medical Instruments Corp.

Decision Date1997-12-17

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

MINI FORCEPS WITH HF, 3.5MM; MICRO FORCEPS WITH HF, 2MM is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 1997-12-17 under 510(k) number K973648. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINI FORCEPS WITH HF, 3.5MM; MICRO FORCEPS WITH HF, 2MM?

MINI FORCEPS WITH HF, 3.5MM; MICRO FORCEPS WITH HF, 2MM is a medical device that received FDA 510(k) clearance on 1997-12-17. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K973648.

When did MINI FORCEPS WITH HF, 3.5MM; MICRO FORCEPS WITH HF, 2MM receive FDA 510(k) clearance?

MINI FORCEPS WITH HF, 3.5MM; MICRO FORCEPS WITH HF, 2MM received FDA 510(k) clearance on 1997-12-17, under 510(k) number K973648.

Who is the listed applicant for MINI FORCEPS WITH HF, 3.5MM; MICRO FORCEPS WITH HF, 2MM?

The FDA 510(k) record lists Richard Wolf Medical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINI FORCEPS WITH HF, 3.5MM; MICRO FORCEPS WITH HF, 2MM?

The FDA product code for MINI FORCEPS WITH HF, 3.5MM; MICRO FORCEPS WITH HF, 2MM is GEI.

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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.