GS-220 HAND IMPAIRMENT EVALUATION SYSTEM— 510(k) K912526

Substantially Equivalent

J-Tech, Inc.

FDA 510(k) clearance K912526 for GS-220 HAND IMPAIRMENT EVALUATION SYSTEM, Substantially Equivalent on 1991-09-05. Applicant: J-Tech, Inc..

Clearance details

Applicant: J-Tech, Inc.
Product code: Code LBB
Advisory panel: Orthopedic
Date received: 1991-06-07
Decision date: 1991-09-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Midvale, UT, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.