MILLIPORE DUAL RATE INTRAVENOUS CASSETTE— 510(k) K811432

Name: FDA 510(k) clearance K811432
Creator: U.S. Food and Drug Administration
Published: 1981-07-13

Substantially Equivalent

Millipore Corp.

FDA 510(k) clearance K811432 for MILLIPORE DUAL RATE INTRAVENOUS CASSETTE, Substantially Equivalent on 1981-07-13. Applicant: Millipore Corp.. Device class: 2.

Clearance details

Applicant: Millipore Corp.
Product code: Code LDR
Device class: Class 2
Regulation: 21 CFR 880.5725
Advisory panel: General Hospital
Date received: 1981-05-22
Decision date: 1981-07-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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