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FDA 510(k)

AESTHESIOMETER

K-Number: K761133 · 1976-12-02

ApplicantFred Sammons, Inc.
Decision Date1976-12-02
Product CodeGXB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

AESTHESIOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Fred Sammons, Inc.. It received FDA 510(k) clearance on 1976-12-02 under 510(k) number K761133. 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 AESTHESIOMETER?

AESTHESIOMETER is a medical device that received FDA 510(k) clearance on 1976-12-02. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K761133.

When did AESTHESIOMETER receive FDA 510(k) clearance?

AESTHESIOMETER received FDA 510(k) clearance on 1976-12-02, under 510(k) number K761133.

Who is the listed applicant for AESTHESIOMETER?

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

What is the FDA product code for AESTHESIOMETER?

The FDA product code for AESTHESIOMETER is GXB.

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Other records listing Fred Sammons, Inc. as applicant

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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.K771847TEMP-TESTERJablecki, Charles, Dr.

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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