INTERFACE ARTERIAL BLOOD FILTER, MODEL 42— 510(k) K862591

Name: FDA 510(k) clearance K862591
Creator: U.S. Food and Drug Administration
Published: 1986-09-04

Substantially Equivalent

Medical, Inc.

FDA 510(k) clearance K862591 for INTERFACE ARTERIAL BLOOD FILTER, MODEL 42, Substantially Equivalent on 1986-09-04. Applicant: Medical, Inc.. Device class: 2.

Clearance details

Applicant: Medical, Inc.
Product code: Code DTM
Device class: Class 2
Regulation: 21 CFR 870.4260
Advisory panel: Cardiovascular
Date received: 1986-07-07
Decision date: 1986-09-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Inver Grove Heights, MN, US

Download summary PDF View on FDA.gov ↗

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