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

Substantially Equivalent

Boehringer Laboratories

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

Clearance details

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

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