FDA 510(k)

#500 SERIES FORCEPS W/CUT/COAGULATE SWITCHES

K-Number: K885199 · 1989-01-13

Decision Date1989-01-13

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

#500 SERIES FORCEPS W/CUT/COAGULATE SWITCHES is the device name listed in this FDA 510(k) record. The listed applicant is Olsen Electrosurgical, Inc.. It received FDA 510(k) clearance on 1989-01-13 under 510(k) number K885199. 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 #500 SERIES FORCEPS W/CUT/COAGULATE SWITCHES?

#500 SERIES FORCEPS W/CUT/COAGULATE SWITCHES is a medical device that received FDA 510(k) clearance on 1989-01-13. The listed applicant is Olsen Electrosurgical, Inc.. The 510(k) number is K885199.

When did #500 SERIES FORCEPS W/CUT/COAGULATE SWITCHES receive FDA 510(k) clearance?

#500 SERIES FORCEPS W/CUT/COAGULATE SWITCHES received FDA 510(k) clearance on 1989-01-13, under 510(k) number K885199.

Who is the listed applicant for #500 SERIES FORCEPS W/CUT/COAGULATE SWITCHES?

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

What is the FDA product code for #500 SERIES FORCEPS W/CUT/COAGULATE SWITCHES?

The FDA product code for #500 SERIES FORCEPS W/CUT/COAGULATE SWITCHES is GEI.

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Other records listing Olsen Electrosurgical, 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.