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FDA 510(k)

DIGITAL GRIP/PINCH STRENGTH METOR

K-Number: K850697 · 1985-05-14

ApplicantChattanooga Group, Inc.
Decision Date1985-05-14
Product CodeLBB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DIGITAL GRIP/PINCH STRENGTH METOR is the device name listed in this FDA 510(k) record. The listed applicant is Chattanooga Group, Inc.. It received FDA 510(k) clearance on 1985-05-14 under 510(k) number K850697. The device is classified under product code LBB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITAL GRIP/PINCH STRENGTH METOR?

DIGITAL GRIP/PINCH STRENGTH METOR is a medical device that received FDA 510(k) clearance on 1985-05-14. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K850697.

When did DIGITAL GRIP/PINCH STRENGTH METOR receive FDA 510(k) clearance?

DIGITAL GRIP/PINCH STRENGTH METOR received FDA 510(k) clearance on 1985-05-14, under 510(k) number K850697.

Who is the listed applicant for DIGITAL GRIP/PINCH STRENGTH METOR?

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

What is the FDA product code for DIGITAL GRIP/PINCH STRENGTH METOR?

The FDA product code for DIGITAL GRIP/PINCH STRENGTH METOR is LBB.

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Other records listing Chattanooga Group, Inc. as applicant

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Related Devices (Code: LBB)

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.

K162412Hoggan Scientific® microFET2™Hoggan Scientific, LLCK073154FACTS HAND AND PINCH GRIP COMBOGlobal Services Group, LLCK052309DIGITAL HAND DYNAMOMETER, MODEL SH5003; DIGITAL PINCH GAUGE, MODEL SH5006Saehan Corp.K042889DYNAMOMETER - MODEL FCE AND MODEL MSCAmetekK012492KADANCE 2000Kada Research, Inc.K981730DIGIT-GRIP WITH LCD, MODEL NUMBER DGR 002Nk Biotechnical Corp.

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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