FDA 510(k)

DISPOSIBLE ELECTRO COAGULATION PROBE

K-Number: K924057 · 1994-03-11

Decision Date1994-03-11

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

DISPOSIBLE ELECTRO COAGULATION PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Endoscopic Technologies, Inc.. It received FDA 510(k) clearance on 1994-03-11 under 510(k) number K924057. 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 DISPOSIBLE ELECTRO COAGULATION PROBE?

DISPOSIBLE ELECTRO COAGULATION PROBE is a medical device that received FDA 510(k) clearance on 1994-03-11. The listed applicant is Endoscopic Technologies, Inc.. The 510(k) number is K924057.

When did DISPOSIBLE ELECTRO COAGULATION PROBE receive FDA 510(k) clearance?

DISPOSIBLE ELECTRO COAGULATION PROBE received FDA 510(k) clearance on 1994-03-11, under 510(k) number K924057.

Who is the listed applicant for DISPOSIBLE ELECTRO COAGULATION PROBE?

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

What is the FDA product code for DISPOSIBLE ELECTRO COAGULATION PROBE?

The FDA product code for DISPOSIBLE ELECTRO COAGULATION PROBE is GEI.

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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.