FDA 510(k)

CAMERON-MILLER MODEL 80-2701, BIPOLAR COAGULATOR

K-Number: K853972 · 1986-01-24

Decision Date1986-01-24

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

CAMERON-MILLER MODEL 80-2701, BIPOLAR COAGULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Cameron-Miller, Inc.. It received FDA 510(k) clearance on 1986-01-24 under 510(k) number K853972. 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 CAMERON-MILLER MODEL 80-2701, BIPOLAR COAGULATOR?

CAMERON-MILLER MODEL 80-2701, BIPOLAR COAGULATOR is a medical device that received FDA 510(k) clearance on 1986-01-24. The listed applicant is Cameron-Miller, Inc.. The 510(k) number is K853972.

When did CAMERON-MILLER MODEL 80-2701, BIPOLAR COAGULATOR receive FDA 510(k) clearance?

CAMERON-MILLER MODEL 80-2701, BIPOLAR COAGULATOR received FDA 510(k) clearance on 1986-01-24, under 510(k) number K853972.

Who is the listed applicant for CAMERON-MILLER MODEL 80-2701, BIPOLAR COAGULATOR?

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

What is the FDA product code for CAMERON-MILLER MODEL 80-2701, BIPOLAR COAGULATOR?

The FDA product code for CAMERON-MILLER MODEL 80-2701, BIPOLAR COAGULATOR is GEI.

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Other records listing Cameron-Miller, Inc. as applicant

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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.