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FDA 510(k)

ELECTROCAUTERY CABLE, BOVIE(TM)/BANANA PLUGS

K-Number: K911365 · 1991-06-11

ApplicantNorthgate Technologies, Inc.
Decision Date1991-06-11
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTROCAUTERY CABLE, BOVIE(TM)/BANANA PLUGS is the device name listed in this FDA 510(k) record. The listed applicant is Northgate Technologies, Inc.. It received FDA 510(k) clearance on 1991-06-11 under 510(k) number K911365. 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 ELECTROCAUTERY CABLE, BOVIE(TM)/BANANA PLUGS?

ELECTROCAUTERY CABLE, BOVIE(TM)/BANANA PLUGS is a medical device that received FDA 510(k) clearance on 1991-06-11. The listed applicant is Northgate Technologies, Inc.. The 510(k) number is K911365.

When did ELECTROCAUTERY CABLE, BOVIE(TM)/BANANA PLUGS receive FDA 510(k) clearance?

ELECTROCAUTERY CABLE, BOVIE(TM)/BANANA PLUGS received FDA 510(k) clearance on 1991-06-11, under 510(k) number K911365.

Who is the listed applicant for ELECTROCAUTERY CABLE, BOVIE(TM)/BANANA PLUGS?

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

What is the FDA product code for ELECTROCAUTERY CABLE, BOVIE(TM)/BANANA PLUGS?

The FDA product code for ELECTROCAUTERY CABLE, BOVIE(TM)/BANANA PLUGS is GEI.

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Related Devices (Code: 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.

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