VASCULAR RECORDER #301— 510(k) K832369

Name: FDA 510(k) clearance K832369
Creator: U.S. Food and Drug Administration
Published: 1984-03-12

Substantially Equivalent

Imex Medical Systems, Inc.

FDA 510(k) clearance K832369 for VASCULAR RECORDER #301, Substantially Equivalent on 1984-03-12. Applicant: Imex Medical Systems, Inc.. Device class: 2.

Clearance details

Applicant: Imex Medical Systems, Inc.
Product code: Code JOP
Device class: Class 2
Regulation: 21 CFR 870.2880
Advisory panel: Cardiovascular
Date received: 1983-07-15
Decision date: 1984-03-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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