ULTIPOR PRE-BYPASS PLUS FILTER W/POSIDYNE MEMBRANE— 510(k) K875094

Name: FDA 510(k) clearance K875094
Creator: U.S. Food and Drug Administration
Published: 1988-02-29

Substantially Equivalent

Pall Biomedical Products Co.

FDA 510(k) clearance K875094 for ULTIPOR PRE-BYPASS PLUS FILTER W/POSIDYNE MEMBRANE, Substantially Equivalent on 1988-02-29. Applicant: Pall Biomedical Products Co.. Device class: 2.

Clearance details

Applicant: Pall Biomedical Products Co.
Product code: Code KRJ
Device class: Class 2
Regulation: 21 CFR 870.4280
Advisory panel: Cardiovascular
Date received: 1987-12-10
Decision date: 1988-02-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Glen Cove, NY, US

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