PREHENSILE HAND— 510(k) K791931

Name: FDA 510(k) clearance K791931
Creator: U.S. Food and Drug Administration
Published: 1979-10-04

Substantially Equivalent

Therapeutic Recreation Systems, Inc.

FDA 510(k) clearance K791931 for PREHENSILE HAND, Substantially Equivalent on 1979-10-04. Applicant: Therapeutic Recreation Systems, Inc.. Device class: 1.

Clearance details

Applicant: Therapeutic Recreation Systems, Inc.
Product code: Code IRA
Device class: Class 1
Regulation: 21 CFR 890.3420
Advisory panel: Physical Medicine
Date received: 1979-09-27
Decision date: 1979-10-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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