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FDA 510(k)

DESERET CAPACITY PLUS ELECTROSURG. PAD

K-Number: K821356 · 1982-07-14

ApplicantWarner-Lambert Co.
Decision Date1982-07-14
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DESERET CAPACITY PLUS ELECTROSURG. PAD is the device name listed in this FDA 510(k) record. The listed applicant is Warner-Lambert Co.. It received FDA 510(k) clearance on 1982-07-14 under 510(k) number K821356. 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 DESERET CAPACITY PLUS ELECTROSURG. PAD?

DESERET CAPACITY PLUS ELECTROSURG. PAD is a medical device that received FDA 510(k) clearance on 1982-07-14. The listed applicant is Warner-Lambert Co.. The 510(k) number is K821356.

When did DESERET CAPACITY PLUS ELECTROSURG. PAD receive FDA 510(k) clearance?

DESERET CAPACITY PLUS ELECTROSURG. PAD received FDA 510(k) clearance on 1982-07-14, under 510(k) number K821356.

Who is the listed applicant for DESERET CAPACITY PLUS ELECTROSURG. PAD?

The FDA 510(k) record lists Warner-Lambert Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DESERET CAPACITY PLUS ELECTROSURG. PAD?

The FDA product code for DESERET CAPACITY PLUS ELECTROSURG. PAD 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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