POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTER— 510(k) K982385

Name: FDA 510(k) clearance K982385
Creator: U.S. Food and Drug Administration
Published: 1999-02-01

Substantially Equivalent

Porous Media Corp.

FDA 510(k) clearance K982385 for POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTER, Substantially Equivalent on 1999-02-01. Applicant: Porous Media Corp.. Device class: 2.

Clearance details

Applicant: Porous Media Corp.
Product code: Code KRJ
Device class: Class 2
Regulation: 21 CFR 870.4280
Advisory panel: Cardiovascular
Date received: 1998-07-09
Decision date: 1999-02-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

Download summary PDF View on FDA.gov ↗

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