BOEHRINGER MRI SUCTION REGULATORY— 510(k) K013976

Name: FDA 510(k) clearance K013976
Creator: U.S. Food and Drug Administration
Published: 2002-01-08

Substantially Equivalent

Boehringer Laboratories

FDA 510(k) clearance K013976 for BOEHRINGER MRI SUCTION REGULATORY, Substantially Equivalent on 2002-01-08. 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: 2001-12-03
Decision date: 2002-01-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norristown, PA, US

Download summary PDF View on FDA.gov ↗

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