IPAG MICRONOVA INTERFACE #781111— 510(k) K791753

Name: FDA 510(k) clearance K791753
Creator: U.S. Food and Drug Administration
Published: 1979-10-02

Substantially Equivalent

Robinton Corp.

FDA 510(k) clearance K791753 for IPAG MICRONOVA INTERFACE #781111, Substantially Equivalent on 1979-10-02. Applicant: Robinton Corp.. Device class: 2.

Clearance details

Applicant: Robinton Corp.
Product code: Code DXG
Device class: Class 2
Regulation: 21 CFR 870.1435
Advisory panel: Cardiovascular
Date received: 1979-09-05
Decision date: 1979-10-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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