SUCTION REGULATOR 7700 SERIES— 510(k) K850200

Substantially Equivalent

Boehringer Laboratories

FDA 510(k) clearance K850200 for SUCTION REGULATOR 7700 SERIES, Substantially Equivalent on 1985-03-04. Applicant: Boehringer Laboratories.

Clearance details

Applicant: Boehringer Laboratories
Product code: Code KDP
Advisory panel: General Hospital
Date received: 1985-01-18
Decision date: 1985-03-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norristown, PA, US

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