CUSHMAN MANUFACTURING, INC. ULTRA 6.0.— 510(k) K960802

Substantially Equivalent

Cushman Mfg., Inc.

FDA 510(k) clearance K960802 for CUSHMAN MANUFACTURING, INC. ULTRA 6.0., Substantially Equivalent on 1996-06-18. Applicant: Cushman Mfg., Inc..

Clearance details

Applicant: Cushman Mfg., Inc.
Product code: Code IMI
Advisory panel: Physical Medicine
Date received: 1996-02-27
Decision date: 1996-06-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Long Beach, CA, US

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