TOTAL FINGER FLEXION SPLINT
K-Number: K822651 · 1982-09-17
Advertisement
Device Summary
Frequently Asked Questions
What is the TOTAL FINGER FLEXION SPLINT?
TOTAL FINGER FLEXION SPLINT is a medical device that received FDA 510(k) clearance on 1982-09-17. The listed applicant is Alimed, Inc.. The 510(k) number is K822651.
When did TOTAL FINGER FLEXION SPLINT receive FDA 510(k) clearance?
TOTAL FINGER FLEXION SPLINT received FDA 510(k) clearance on 1982-09-17, under 510(k) number K822651.
Who is the listed applicant for TOTAL FINGER FLEXION SPLINT?
The FDA 510(k) record lists Alimed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TOTAL FINGER FLEXION SPLINT?
The FDA product code for TOTAL FINGER FLEXION 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 Alimed, 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.
Advertisement