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FDA 510(k)

BK-7531 PAIN THRESHOLD/FINGER FORCE GAUG

K-Number: K801719 · 1980-08-04

ApplicantFred Sammons, Inc.
Decision Date1980-08-04
Product CodeHRW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BK-7531 PAIN THRESHOLD/FINGER FORCE GAUG 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 1980-08-04 under 510(k) number K801719. The device is classified under product code HRW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BK-7531 PAIN THRESHOLD/FINGER FORCE GAUG?

BK-7531 PAIN THRESHOLD/FINGER FORCE GAUG is a medical device that received FDA 510(k) clearance on 1980-08-04. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K801719.

When did BK-7531 PAIN THRESHOLD/FINGER FORCE GAUG receive FDA 510(k) clearance?

BK-7531 PAIN THRESHOLD/FINGER FORCE GAUG received FDA 510(k) clearance on 1980-08-04, under 510(k) number K801719.

Who is the listed applicant for BK-7531 PAIN THRESHOLD/FINGER FORCE GAUG?

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 BK-7531 PAIN THRESHOLD/FINGER FORCE GAUG?

The FDA product code for BK-7531 PAIN THRESHOLD/FINGER FORCE GAUG is HRW.

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Other records listing Fred Sammons, Inc. as applicant

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Related Devices (Code: HRW)

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.

K971407JTECH COMMANDER AND ALGOMETERJ-Tech Medical, Inc.K970870DIGIT-GRIP WITH LCD (DGR002)Nk Biotechnical Corp.K894557LIGHTSCOPE SETOptikK861396HANDHELD DYNAMOMETER, MODEL #160 AND #111Spark Instruments & Academics, Inc.K821631PINCH GAUGE, 0-301 LBS.Fred Sammons, Inc.K812343PINCH METERFred 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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