PARENTERAL INFUSION CONTROLLER, ELEC.— 510(k) K780106

Name: FDA 510(k) clearance K780106
Creator: U.S. Food and Drug Administration
Published: 1978-02-21

Substantially Equivalent

National Patent Development Corp.

FDA 510(k) clearance K780106 for PARENTERAL INFUSION CONTROLLER, ELEC., Substantially Equivalent on 1978-02-21. Applicant: National Patent Development Corp.. Device class: 2.

Clearance details

Applicant: National Patent Development Corp.
Product code: Code FLN
Device class: Class 2
Regulation: 21 CFR 880.2420
Advisory panel: General Hospital
Date received: 1978-01-20
Decision date: 1978-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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