PEDICRAFT INFANT REFLUX WEDGE— 510(k) K905629

Substantially Equivalent

Pedicraft, Inc.

FDA 510(k) clearance K905629 for PEDICRAFT INFANT REFLUX WEDGE, Substantially Equivalent on 1991-03-13. Applicant: Pedicraft, Inc..

Clearance details

Applicant: Pedicraft, Inc.
Product code: Code FRP
Advisory panel: General Hospital
Date received: 1990-12-14
Decision date: 1991-03-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jacksonville, FL, US

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