INFUSION CONTROLLER, PARENTERAL— 510(k) K781216

Name: FDA 510(k) clearance K781216
Creator: U.S. Food and Drug Administration
Published: 1978-08-10

Substantially Equivalent

National Patent Development Corp.

FDA 510(k) clearance K781216 for INFUSION CONTROLLER, PARENTERAL, Substantially Equivalent on 1978-08-10. Applicant: National Patent Development Corp.. Device class: 2.

Clearance details

Applicant: National Patent Development Corp.
Product code: Code FLS
Device class: Class 2
Regulation: 21 CFR 868.2377
Advisory panel: Anesthesiology
Date received: 1978-07-17
Decision date: 1978-08-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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