SURGICAL VESSEL DILATORS-CATHERIZA-— 510(k) K833676

Name: FDA 510(k) clearance K833676
Creator: U.S. Food and Drug Administration
Published: 1984-03-19

Substantially Equivalent

Cimed Intl., Inc.

FDA 510(k) clearance K833676 for SURGICAL VESSEL DILATORS-CATHERIZA-, Substantially Equivalent on 1984-03-19. Applicant: Cimed Intl., Inc.. Device class: 2.

Clearance details

Applicant: Cimed Intl., Inc.
Product code: Code DWP
Device class: Class 2
Regulation: 21 CFR 870.4475
Advisory panel: Cardiovascular
Date received: 1983-10-14
Decision date: 1984-03-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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