PREPACELL-STERILE-BONE MARROW ASPIR— 510(k) K833438

Substantially Equivalent

Applied Medical Devices, Inc.

FDA 510(k) clearance K833438 for PREPACELL-STERILE-BONE MARROW ASPIR, Substantially Equivalent on 1984-02-09. Applicant: Applied Medical Devices, Inc..

Clearance details

Applicant: Applied Medical Devices, Inc.
Product code: Code KDD
Advisory panel: General, Plastic Surgery
Date received: 1983-10-05
Decision date: 1984-02-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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