PM3000 & PM3100 VACUUM REGULATOR— 510(k) K922817

Substantially Equivalent

Precision Medical, Inc.

FDA 510(k) clearance K922817 for PM3000 & PM3100 VACUUM REGULATOR, Substantially Equivalent on 1993-03-04. Applicant: Precision Medical, Inc..

Clearance details

Applicant: Precision Medical, Inc.
Product code: Code KDP
Advisory panel: General Hospital
Date received: 1992-06-11
Decision date: 1993-03-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Northampton, PA, US

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