GREENLEAF HAND IMPAIRMENT EVALUATION SYSTEM— 510(k) K893537

Name: FDA 510(k) clearance K893537
Creator: U.S. Food and Drug Administration
Published: 1989-10-10

Substantially Equivalent

Greenleaf Medical Systems, Inc.

FDA 510(k) clearance K893537 for GREENLEAF HAND IMPAIRMENT EVALUATION SYSTEM, Substantially Equivalent on 1989-10-10. Applicant: Greenleaf Medical Systems, Inc.. Device class: 2.

Clearance details

Applicant: Greenleaf Medical Systems, Inc.
Product code: Code LBB
Device class: Class 2
Regulation: 21 CFR 888.1240
Advisory panel: Orthopedic
Date received: 1989-05-08
Decision date: 1989-10-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Palo Alto, CA, US

Download summary PDF View on FDA.gov ↗

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K943929 — DATAGLOVE AND MOVEMENT ANALYSIS SYSTEM (MAS)1995-05-15
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K884723 — (DATAGLOVE) HAND IMPAIRMENT EVALUATION SYSTEM1989-02-08

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