BOEHRINGER LABORATORIES SUCTION REGULATOR, MODIFIED— 510(k) K933232

Name: FDA 510(k) clearance K933232
Creator: U.S. Food and Drug Administration
Published: 1994-03-28

Substantially Equivalent

Boehringer Laboratories

FDA 510(k) clearance K933232 for BOEHRINGER LABORATORIES SUCTION REGULATOR, MODIFIED, Substantially Equivalent on 1994-03-28. Applicant: Boehringer Laboratories. Device class: 2.

Clearance details

Applicant: Boehringer Laboratories
Product code: Code KDP
Device class: Class 2
Regulation: 21 CFR 880.6740
Advisory panel: General Hospital
Date received: 1993-07-06
Decision date: 1994-03-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norristown, PA, US

Download summary PDF View on FDA.gov ↗

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