PEDICRAGT BASSINET— 510(k) K925949

Substantially Equivalent

Pedicraft, Inc.

FDA 510(k) clearance K925949 for PEDICRAGT BASSINET, Substantially Equivalent on 1993-04-20. Applicant: Pedicraft, Inc..

Clearance details

Applicant: Pedicraft, Inc.
Product code: Code FMS
Advisory panel: General Hospital
Date received: 1992-11-24
Decision date: 1993-04-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jacksonville, FL, US

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