FDA 510(k)

LECTROSURIGICAL, CUTTING AND COAGULATION AND ACCESSORIES

K-Number: K944681 · 1994-12-22

Decision Date1994-12-22

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

LECTROSURIGICAL, CUTTING AND COAGULATION AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Birtcher Medical Systems, Inc.. It received FDA 510(k) clearance on 1994-12-22 under 510(k) number K944681. 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 LECTROSURIGICAL, CUTTING AND COAGULATION AND ACCESSORIES?

LECTROSURIGICAL, CUTTING AND COAGULATION AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1994-12-22. The listed applicant is Birtcher Medical Systems, Inc.. The 510(k) number is K944681.

When did LECTROSURIGICAL, CUTTING AND COAGULATION AND ACCESSORIES receive FDA 510(k) clearance?

LECTROSURIGICAL, CUTTING AND COAGULATION AND ACCESSORIES received FDA 510(k) clearance on 1994-12-22, under 510(k) number K944681.

Who is the listed applicant for LECTROSURIGICAL, CUTTING AND COAGULATION AND ACCESSORIES?

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

What is the FDA product code for LECTROSURIGICAL, CUTTING AND COAGULATION AND ACCESSORIES?

The FDA product code for LECTROSURIGICAL, CUTTING AND COAGULATION AND ACCESSORIES is GEI.

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Other records listing Birtcher Medical Systems, 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.