FDA 510(k)

VALLEYLAB MACROBIPOLAR FORCEPS HANDPIECE, E3200

K-Number: K926414 · 1993-05-17

Decision Date1993-05-17

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

VALLEYLAB MACROBIPOLAR FORCEPS HANDPIECE, E3200 is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1993-05-17 under 510(k) number K926414. 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 VALLEYLAB MACROBIPOLAR FORCEPS HANDPIECE, E3200?

VALLEYLAB MACROBIPOLAR FORCEPS HANDPIECE, E3200 is a medical device that received FDA 510(k) clearance on 1993-05-17. The listed applicant is Valleylab, Inc.. The 510(k) number is K926414.

When did VALLEYLAB MACROBIPOLAR FORCEPS HANDPIECE, E3200 receive FDA 510(k) clearance?

VALLEYLAB MACROBIPOLAR FORCEPS HANDPIECE, E3200 received FDA 510(k) clearance on 1993-05-17, under 510(k) number K926414.

Who is the listed applicant for VALLEYLAB MACROBIPOLAR FORCEPS HANDPIECE, E3200?

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

What is the FDA product code for VALLEYLAB MACROBIPOLAR FORCEPS HANDPIECE, E3200?

The FDA product code for VALLEYLAB MACROBIPOLAR FORCEPS HANDPIECE, E3200 is GEI.

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Other records listing Valleylab, Inc. as applicant

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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.