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FDA 510(k)

BOVIE 400-CT ELECTROSURGICAL GENERATOR (UNIT)

K-Number: K872705 · 1987-09-01

ApplicantClinical Technology Corp.
Decision Date1987-09-01
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BOVIE 400-CT ELECTROSURGICAL GENERATOR (UNIT) is the device name listed in this FDA 510(k) record. The listed applicant is Clinical Technology Corp.. It received FDA 510(k) clearance on 1987-09-01 under 510(k) number K872705. 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 400-CT ELECTROSURGICAL GENERATOR (UNIT)?

BOVIE 400-CT ELECTROSURGICAL GENERATOR (UNIT) is a medical device that received FDA 510(k) clearance on 1987-09-01. The listed applicant is Clinical Technology Corp.. The 510(k) number is K872705.

When did BOVIE 400-CT ELECTROSURGICAL GENERATOR (UNIT) receive FDA 510(k) clearance?

BOVIE 400-CT ELECTROSURGICAL GENERATOR (UNIT) received FDA 510(k) clearance on 1987-09-01, under 510(k) number K872705.

Who is the listed applicant for BOVIE 400-CT ELECTROSURGICAL GENERATOR (UNIT)?

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

What is the FDA product code for BOVIE 400-CT ELECTROSURGICAL GENERATOR (UNIT)?

The FDA product code for BOVIE 400-CT ELECTROSURGICAL GENERATOR (UNIT) is GEI.

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Other records listing Clinical Technology Corp. 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.

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