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FDA 510(k)

TEMP-TESTER

K-Number: K771847 · 1977-11-02

ApplicantJablecki, Charles, Dr.
Decision Date1977-11-02
Product CodeGXB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TEMP-TESTER is the device name listed in this FDA 510(k) record. The listed applicant is Jablecki, Charles, Dr.. It received FDA 510(k) clearance on 1977-11-02 under 510(k) number K771847. The device is classified under product code GXB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEMP-TESTER?

TEMP-TESTER is a medical device that received FDA 510(k) clearance on 1977-11-02. The listed applicant is Jablecki, Charles, Dr.. The 510(k) number is K771847.

When did TEMP-TESTER receive FDA 510(k) clearance?

TEMP-TESTER received FDA 510(k) clearance on 1977-11-02, under 510(k) number K771847.

Who is the listed applicant for TEMP-TESTER?

The FDA 510(k) record lists Jablecki, Charles, Dr. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TEMP-TESTER?

The FDA product code for TEMP-TESTER is GXB.

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Related Devices (Code: GXB)

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.

K933798NU-PREP GELCadwell Laboratories, Inc.K871571NEUROTIPS(TM)Ulster Scientific, Inc.K801907ALGESIOMETERRowan Products, Inc.K772406AESTHESIOMETERFred Sammons, Inc.K761133AESTHESIOMETERFred Sammons, Inc.

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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