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FDA 510(k)

CAVITRON ELECTROSURGICAL MODULE (CEM) AND PAK

K-Number: K881687 · 1988-06-20

ApplicantCavitron Surgical Systems
Decision Date1988-06-20
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CAVITRON ELECTROSURGICAL MODULE (CEM) AND PAK is the device name listed in this FDA 510(k) record. The listed applicant is Cavitron Surgical Systems. It received FDA 510(k) clearance on 1988-06-20 under 510(k) number K881687. 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 CAVITRON ELECTROSURGICAL MODULE (CEM) AND PAK?

CAVITRON ELECTROSURGICAL MODULE (CEM) AND PAK is a medical device that received FDA 510(k) clearance on 1988-06-20. The listed applicant is Cavitron Surgical Systems. The 510(k) number is K881687.

When did CAVITRON ELECTROSURGICAL MODULE (CEM) AND PAK receive FDA 510(k) clearance?

CAVITRON ELECTROSURGICAL MODULE (CEM) AND PAK received FDA 510(k) clearance on 1988-06-20, under 510(k) number K881687.

Who is the listed applicant for CAVITRON ELECTROSURGICAL MODULE (CEM) AND PAK?

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

What is the FDA product code for CAVITRON ELECTROSURGICAL MODULE (CEM) AND PAK?

The FDA product code for CAVITRON ELECTROSURGICAL MODULE (CEM) AND PAK is GEI.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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