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FDA 510(k)

BOVIE CSV HAND CONTROL ADAPTER

K-Number: K791767 · 1979-10-11

ApplicantSybron Corp.
Decision Date1979-10-11
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BOVIE CSV HAND CONTROL ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Sybron Corp.. It received FDA 510(k) clearance on 1979-10-11 under 510(k) number K791767. 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 CSV HAND CONTROL ADAPTER?

BOVIE CSV HAND CONTROL ADAPTER is a medical device that received FDA 510(k) clearance on 1979-10-11. The listed applicant is Sybron Corp.. The 510(k) number is K791767.

When did BOVIE CSV HAND CONTROL ADAPTER receive FDA 510(k) clearance?

BOVIE CSV HAND CONTROL ADAPTER received FDA 510(k) clearance on 1979-10-11, under 510(k) number K791767.

Who is the listed applicant for BOVIE CSV HAND CONTROL ADAPTER?

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

What is the FDA product code for BOVIE CSV HAND CONTROL ADAPTER?

The FDA product code for BOVIE CSV HAND CONTROL ADAPTER 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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