DMG100 AND 500 ISOMETRIC STRENGTH DYNAMOMETER
K-Number: K923262 · 1992-10-27
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Device Summary
Frequently Asked Questions
What is the DMG100 AND 500 ISOMETRIC STRENGTH DYNAMOMETER?
DMG100 AND 500 ISOMETRIC STRENGTH DYNAMOMETER is a medical device that received FDA 510(k) clearance on 1992-10-27. The listed applicant is John Chatillon & Sons, Inc.. The 510(k) number is K923262.
When did DMG100 AND 500 ISOMETRIC STRENGTH DYNAMOMETER receive FDA 510(k) clearance?
DMG100 AND 500 ISOMETRIC STRENGTH DYNAMOMETER received FDA 510(k) clearance on 1992-10-27, under 510(k) number K923262.
Who is the listed applicant for DMG100 AND 500 ISOMETRIC STRENGTH 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 DMG100 AND 500 ISOMETRIC STRENGTH DYNAMOMETER?
The FDA product code for DMG100 AND 500 ISOMETRIC STRENGTH 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.
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.
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.
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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