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FDA 510(k)

SYBRON BOVIE CSV HAND CONTR. ELECTROSURG

K-Number: K820494 · 1982-04-09

ApplicantSybron Corp.
Decision Date1982-04-09
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SYBRON BOVIE CSV HAND CONTR. ELECTROSURG is the device name listed in this FDA 510(k) record. The listed applicant is Sybron Corp.. It received FDA 510(k) clearance on 1982-04-09 under 510(k) number K820494. 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 SYBRON BOVIE CSV HAND CONTR. ELECTROSURG?

SYBRON BOVIE CSV HAND CONTR. ELECTROSURG is a medical device that received FDA 510(k) clearance on 1982-04-09. The listed applicant is Sybron Corp.. The 510(k) number is K820494.

When did SYBRON BOVIE CSV HAND CONTR. ELECTROSURG receive FDA 510(k) clearance?

SYBRON BOVIE CSV HAND CONTR. ELECTROSURG received FDA 510(k) clearance on 1982-04-09, under 510(k) number K820494.

Who is the listed applicant for SYBRON BOVIE CSV HAND CONTR. ELECTROSURG?

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 SYBRON BOVIE CSV HAND CONTR. ELECTROSURG?

The FDA product code for SYBRON BOVIE CSV HAND CONTR. ELECTROSURG 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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