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FDA 510(k)

MULTIPERFECTEMP

K-Number: K820902 · 1982-04-26

ApplicantKay Medical, Inc.
Decision Date1982-04-26
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MULTIPERFECTEMP is the device name listed in this FDA 510(k) record. The listed applicant is Kay Medical, Inc.. It received FDA 510(k) clearance on 1982-04-26 under 510(k) number K820902. 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 MULTIPERFECTEMP?

MULTIPERFECTEMP is a medical device that received FDA 510(k) clearance on 1982-04-26. The listed applicant is Kay Medical, Inc.. The 510(k) number is K820902.

When did MULTIPERFECTEMP receive FDA 510(k) clearance?

MULTIPERFECTEMP received FDA 510(k) clearance on 1982-04-26, under 510(k) number K820902.

Who is the listed applicant for MULTIPERFECTEMP?

The FDA 510(k) record lists Kay Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTIPERFECTEMP?

The FDA product code for MULTIPERFECTEMP is GEI.

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Related Devices (Code: GEI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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