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FDA 510(k)

BIRTCHER FOOTCONTROLLED SUCTION COAGULATOR

K-Number: K900347 · 1990-04-10

ApplicantBirtcher Electro Medical Systems
Decision Date1990-04-10
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BIRTCHER FOOTCONTROLLED SUCTION COAGULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Birtcher Electro Medical Systems. It received FDA 510(k) clearance on 1990-04-10 under 510(k) number K900347. 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 BIRTCHER FOOTCONTROLLED SUCTION COAGULATOR?

BIRTCHER FOOTCONTROLLED SUCTION COAGULATOR is a medical device that received FDA 510(k) clearance on 1990-04-10. The listed applicant is Birtcher Electro Medical Systems. The 510(k) number is K900347.

When did BIRTCHER FOOTCONTROLLED SUCTION COAGULATOR receive FDA 510(k) clearance?

BIRTCHER FOOTCONTROLLED SUCTION COAGULATOR received FDA 510(k) clearance on 1990-04-10, under 510(k) number K900347.

Who is the listed applicant for BIRTCHER FOOTCONTROLLED SUCTION COAGULATOR?

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

What is the FDA product code for BIRTCHER FOOTCONTROLLED SUCTION COAGULATOR?

The FDA product code for BIRTCHER FOOTCONTROLLED SUCTION COAGULATOR 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.

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