PM3000 & PM3100 VACUUM REGULATOR— 510(k) K922817

Name: FDA 510(k) clearance K922817
Creator: U.S. Food and Drug Administration
Published: 1993-03-04

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.. Device class: 2.

Clearance details

Applicant: Precision Medical, Inc.
Product code: Code KDP
Device class: Class 2
Regulation: 21 CFR 880.6740
Advisory panel: General Hospital
Date received: 1992-06-11
Decision date: 1993-03-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Northampton, PA, US

Download summary PDF View on FDA.gov ↗

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