PM3300 INTERMITTENT VACUUM— 510(k) K944479

Name: FDA 510(k) clearance K944479
Creator: U.S. Food and Drug Administration
Published: 1994-12-22

Substantially Equivalent

Precision Medical, Inc.

FDA 510(k) clearance K944479 for PM3300 INTERMITTENT VACUUM, Substantially Equivalent on 1994-12-22. 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: 1994-09-13
Decision date: 1994-12-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Northampton, PA, US

Download summary PDF View on FDA.gov ↗

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