FDA 510(k)

GRASPING FORCEPS, RIGHT AND LEFT CURVED

K-Number: K972519 · 1997-09-08

ApplicantRichard Wolf Medical Instruments Corp.

Decision Date1997-09-08

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

GRASPING FORCEPS, RIGHT AND LEFT CURVED 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 1997-09-08 under 510(k) number K972519. 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 GRASPING FORCEPS, RIGHT AND LEFT CURVED?

GRASPING FORCEPS, RIGHT AND LEFT CURVED is a medical device that received FDA 510(k) clearance on 1997-09-08. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K972519.

When did GRASPING FORCEPS, RIGHT AND LEFT CURVED receive FDA 510(k) clearance?

GRASPING FORCEPS, RIGHT AND LEFT CURVED received FDA 510(k) clearance on 1997-09-08, under 510(k) number K972519.

Who is the listed applicant for GRASPING FORCEPS, RIGHT AND LEFT CURVED?

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 GRASPING FORCEPS, RIGHT AND LEFT CURVED?

The FDA product code for GRASPING FORCEPS, RIGHT AND LEFT CURVED 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.