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FDA 510(k)

CLINCAL HAND MASTER SYSTEM MODEL # EXH9000-002

K-Number: K922940 · 1992-10-05

ApplicantExos, Inc.
Decision Date1992-10-05
Product CodeLBB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CLINCAL HAND MASTER SYSTEM MODEL # EXH9000-002 is the device name listed in this FDA 510(k) record. The listed applicant is Exos, Inc.. It received FDA 510(k) clearance on 1992-10-05 under 510(k) number K922940. 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 CLINCAL HAND MASTER SYSTEM MODEL # EXH9000-002?

CLINCAL HAND MASTER SYSTEM MODEL # EXH9000-002 is a medical device that received FDA 510(k) clearance on 1992-10-05. The listed applicant is Exos, Inc.. The 510(k) number is K922940.

When did CLINCAL HAND MASTER SYSTEM MODEL # EXH9000-002 receive FDA 510(k) clearance?

CLINCAL HAND MASTER SYSTEM MODEL # EXH9000-002 received FDA 510(k) clearance on 1992-10-05, under 510(k) number K922940.

Who is the listed applicant for CLINCAL HAND MASTER SYSTEM MODEL # EXH9000-002?

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

What is the FDA product code for CLINCAL HAND MASTER SYSTEM MODEL # EXH9000-002?

The FDA product code for CLINCAL HAND MASTER SYSTEM MODEL # EXH9000-002 is LBB.

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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

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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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