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FDA 510(k)

MIRROR FINISH BIPOLAR FORCEPS

K-Number: K963499 · 1996-10-08

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1996-10-08
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MIRROR FINISH BIPOLAR FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1996-10-08 under 510(k) number K963499. 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 MIRROR FINISH BIPOLAR FORCEPS?

MIRROR FINISH BIPOLAR FORCEPS is a medical device that received FDA 510(k) clearance on 1996-10-08. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K963499.

When did MIRROR FINISH BIPOLAR FORCEPS receive FDA 510(k) clearance?

MIRROR FINISH BIPOLAR FORCEPS received FDA 510(k) clearance on 1996-10-08, under 510(k) number K963499.

Who is the listed applicant for MIRROR FINISH BIPOLAR FORCEPS?

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

What is the FDA product code for MIRROR FINISH BIPOLAR FORCEPS?

The FDA product code for MIRROR FINISH BIPOLAR FORCEPS is GEI.

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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.

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