(DATAGLOVE) HAND IMPAIRMENT EVALUATION SYSTEM— 510(k) K884723

Name: FDA 510(k) clearance K884723
Creator: U.S. Food and Drug Administration
Published: 1989-02-08

Substantially Equivalent

Greenleaf Medical Systems, Inc.

FDA 510(k) clearance K884723 for (DATAGLOVE) HAND IMPAIRMENT EVALUATION SYSTEM, Substantially Equivalent on 1989-02-08. Applicant: Greenleaf Medical Systems, Inc.. Device class: 1.

Clearance details

Applicant: Greenleaf Medical Systems, Inc.
Product code: Code KQX
Device class: Class 1
Regulation: 21 CFR 888.1500
Advisory panel: Orthopedic
Date received: 1988-11-10
Decision date: 1989-02-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Palo Alto, CA, US

Download summary PDF View on FDA.gov ↗

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