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FDA 510(k)

INSTATEMP

K-Number: K770944 · 1977-07-27

ApplicantH.I. Silverman, D.Sc.
Decision Date1977-07-27
Product CodeKDP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INSTATEMP is the device name listed in this FDA 510(k) record. The listed applicant is H.I. Silverman, D.Sc.. It received FDA 510(k) clearance on 1977-07-27 under 510(k) number K770944. The device is classified under product code KDP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSTATEMP?

INSTATEMP is a medical device that received FDA 510(k) clearance on 1977-07-27. The listed applicant is H.I. Silverman, D.Sc.. The 510(k) number is K770944.

When did INSTATEMP receive FDA 510(k) clearance?

INSTATEMP received FDA 510(k) clearance on 1977-07-27, under 510(k) number K770944.

Who is the listed applicant for INSTATEMP?

The FDA 510(k) record lists H.I. Silverman, D.Sc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INSTATEMP?

The FDA product code for INSTATEMP is KDP.

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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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