BOEHRINGER LAB SUCTION INTERRUPTER— 510(k) K853155

Name: FDA 510(k) clearance K853155
Creator: U.S. Food and Drug Administration
Published: 1985-10-16

Substantially Equivalent

Boehringer Laboratories

FDA 510(k) clearance K853155 for BOEHRINGER LAB SUCTION INTERRUPTER, Substantially Equivalent on 1985-10-16. 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: 1985-07-29
Decision date: 1985-10-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norristown, PA, US

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