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FDA 510(k)

CLEV-DENT COLHS ELECTROSURG, MOLEL TR-5

K-Number: K770969 · 1977-06-24

ApplicantCavitron Corp.
Decision Date1977-06-24
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CLEV-DENT COLHS ELECTROSURG, MOLEL TR-5 is the device name listed in this FDA 510(k) record. The listed applicant is Cavitron Corp.. It received FDA 510(k) clearance on 1977-06-24 under 510(k) number K770969. 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 CLEV-DENT COLHS ELECTROSURG, MOLEL TR-5?

CLEV-DENT COLHS ELECTROSURG, MOLEL TR-5 is a medical device that received FDA 510(k) clearance on 1977-06-24. The listed applicant is Cavitron Corp.. The 510(k) number is K770969.

When did CLEV-DENT COLHS ELECTROSURG, MOLEL TR-5 receive FDA 510(k) clearance?

CLEV-DENT COLHS ELECTROSURG, MOLEL TR-5 received FDA 510(k) clearance on 1977-06-24, under 510(k) number K770969.

Who is the listed applicant for CLEV-DENT COLHS ELECTROSURG, MOLEL TR-5?

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

What is the FDA product code for CLEV-DENT COLHS ELECTROSURG, MOLEL TR-5?

The FDA product code for CLEV-DENT COLHS ELECTROSURG, MOLEL TR-5 is GEI.

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Other records listing Cavitron 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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