FDA 510(k)

BIPOLAR FORCEPS SET (MODULAR)

K-Number: K981321 · 1998-07-07

ApplicantRichard Wolf Medical Instruments Corp.

Decision Date1998-07-07

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

BIPOLAR FORCEPS SET (MODULAR) 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 1998-07-07 under 510(k) number K981321. 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 BIPOLAR FORCEPS SET (MODULAR)?

BIPOLAR FORCEPS SET (MODULAR) is a medical device that received FDA 510(k) clearance on 1998-07-07. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K981321.

When did BIPOLAR FORCEPS SET (MODULAR) receive FDA 510(k) clearance?

BIPOLAR FORCEPS SET (MODULAR) received FDA 510(k) clearance on 1998-07-07, under 510(k) number K981321.

Who is the listed applicant for BIPOLAR FORCEPS SET (MODULAR)?

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 BIPOLAR FORCEPS SET (MODULAR)?

The FDA product code for BIPOLAR FORCEPS SET (MODULAR) 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.