TRANS DISTAL JOINT FINGER EXTEN. SPLINT
K-Number: K801714 · 1980-08-07
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Device Summary
Frequently Asked Questions
What is the TRANS DISTAL JOINT FINGER EXTEN. SPLINT?
TRANS DISTAL JOINT FINGER EXTEN. SPLINT is a medical device that received FDA 510(k) clearance on 1980-08-07. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K801714.
When did TRANS DISTAL JOINT FINGER EXTEN. SPLINT receive FDA 510(k) clearance?
TRANS DISTAL JOINT FINGER EXTEN. SPLINT received FDA 510(k) clearance on 1980-08-07, under 510(k) number K801714.
Who is the listed applicant for TRANS DISTAL JOINT FINGER EXTEN. SPLINT?
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 TRANS DISTAL JOINT FINGER EXTEN. SPLINT?
The FDA product code for TRANS DISTAL JOINT FINGER EXTEN. SPLINT 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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