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FDA 510(k)

DYNAMOMETER

K-Number: K964685 · 1997-01-27

ApplicantJohn Chatillon & Sons, Inc.
Decision Date1997-01-27
Product CodeLBB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DYNAMOMETER is the device name listed in this FDA 510(k) record. The listed applicant is John Chatillon & Sons, Inc.. It received FDA 510(k) clearance on 1997-01-27 under 510(k) number K964685. 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 DYNAMOMETER?

DYNAMOMETER is a medical device that received FDA 510(k) clearance on 1997-01-27. The listed applicant is John Chatillon & Sons, Inc.. The 510(k) number is K964685.

When did DYNAMOMETER receive FDA 510(k) clearance?

DYNAMOMETER received FDA 510(k) clearance on 1997-01-27, under 510(k) number K964685.

Who is the listed applicant for DYNAMOMETER?

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

What is the FDA product code for DYNAMOMETER?

The FDA product code for DYNAMOMETER is LBB.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing John Chatillon & Sons, Inc. as applicant

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.

K931321CSD 200/300/400/500 DYNAMOMETERK923262DMG100 AND 500 ISOMETRIC STRENGTH DYNAMOMETER

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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