PARENTERAL INFUSION CONTROLLER— 510(k) K780223

Name: FDA 510(k) clearance K780223
Creator: U.S. Food and Drug Administration
Published: 1978-04-10

Substantially Equivalent

Travenol Laboratories, S.A.

FDA 510(k) clearance K780223 for PARENTERAL INFUSION CONTROLLER, Substantially Equivalent on 1978-04-10. Applicant: Travenol Laboratories, S.A.. Device class: 2.

Clearance details

Applicant: Travenol Laboratories, S.A.
Product code: Code FLN
Device class: Class 2
Regulation: 21 CFR 880.2420
Advisory panel: General Hospital
Date received: 1978-02-09
Decision date: 1978-04-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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