KPP PERITONEAL DIALYSATE FILTER— 510(k) K803275

Name: FDA 510(k) clearance K803275
Creator: U.S. Food and Drug Administration
Published: 1981-03-13

Substantially Equivalent

Millipore Corp.

FDA 510(k) clearance K803275 for KPP PERITONEAL DIALYSATE FILTER, Substantially Equivalent on 1981-03-13. Applicant: Millipore Corp.. Device class: 2.

Clearance details

Applicant: Millipore Corp.
Product code: Code KPP
Device class: Class 2
Regulation: 21 CFR 876.5630
Advisory panel: Gastroenterology, Urology
Date received: 1980-12-29
Decision date: 1981-03-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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