FDA 510(k)

BOVIE ICON GI ELECTROSURGICAL GENERATOR, MODEL GI 120

K-Number: K061884 · 2006-09-06

Decision Date2006-09-06

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

BOVIE ICON GI ELECTROSURGICAL GENERATOR, MODEL GI 120 is the device name listed in this FDA 510(k) record. The listed applicant is Bovie Medical. It received FDA 510(k) clearance on 2006-09-06 under 510(k) number K061884. 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 BOVIE ICON GI ELECTROSURGICAL GENERATOR, MODEL GI 120?

BOVIE ICON GI ELECTROSURGICAL GENERATOR, MODEL GI 120 is a medical device that received FDA 510(k) clearance on 2006-09-06. The listed applicant is Bovie Medical. The 510(k) number is K061884.

When did BOVIE ICON GI ELECTROSURGICAL GENERATOR, MODEL GI 120 receive FDA 510(k) clearance?

BOVIE ICON GI ELECTROSURGICAL GENERATOR, MODEL GI 120 received FDA 510(k) clearance on 2006-09-06, under 510(k) number K061884.

Who is the listed applicant for BOVIE ICON GI ELECTROSURGICAL GENERATOR, MODEL GI 120?

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

What is the FDA product code for BOVIE ICON GI ELECTROSURGICAL GENERATOR, MODEL GI 120?

The FDA product code for BOVIE ICON GI ELECTROSURGICAL GENERATOR, MODEL GI 120 is GEI.

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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.