WRIST SUPPORT
K-Number: K823601 · 1982-12-22
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Device Summary
Frequently Asked Questions
What is the WRIST SUPPORT?
WRIST SUPPORT is a medical device that received FDA 510(k) clearance on 1982-12-22. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K823601.
When did WRIST SUPPORT receive FDA 510(k) clearance?
WRIST SUPPORT received FDA 510(k) clearance on 1982-12-22, under 510(k) number K823601.
Who is the listed applicant for WRIST SUPPORT?
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 WRIST SUPPORT?
The FDA product code for WRIST SUPPORT is ILH.
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 Fred Sammons, 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: ILH)
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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