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FDA 510(k)

BIPOLAR COAGULATION INSTRUMENT

K-Number: K952161 · 1995-07-05

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1995-07-05
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BIPOLAR COAGULATION INSTRUMENT 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 1995-07-05 under 510(k) number K952161. 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 COAGULATION INSTRUMENT?

BIPOLAR COAGULATION INSTRUMENT is a medical device that received FDA 510(k) clearance on 1995-07-05. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K952161.

When did BIPOLAR COAGULATION INSTRUMENT receive FDA 510(k) clearance?

BIPOLAR COAGULATION INSTRUMENT received FDA 510(k) clearance on 1995-07-05, under 510(k) number K952161.

Who is the listed applicant for BIPOLAR COAGULATION INSTRUMENT?

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 BIPOLAR COAGULATION INSTRUMENT?

The FDA product code for BIPOLAR COAGULATION INSTRUMENT 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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