GREENLEAF HAND IMPAIRMENT EVALUATION SYSTEM— 510(k) K893537

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..

Clearance details

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

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