MULTILUMEN INTRAVENOUS INFUSION CATHETER— 510(k) K821220

Name: FDA 510(k) clearance K821220
Creator: U.S. Food and Drug Administration
Published: 1982-07-09

Substantially Equivalent

Clincal Instruments Corp.

FDA 510(k) clearance K821220 for MULTILUMEN INTRAVENOUS INFUSION CATHETER, Substantially Equivalent on 1982-07-09. Applicant: Clincal Instruments Corp.. Device class: 1.

Clearance details

Applicant: Clincal Instruments Corp.
Product code: Code GBP
Device class: Class 1
Regulation: 21 CFR 878.4200
Advisory panel: General, Plastic Surgery
Date received: 1982-04-27
Decision date: 1982-07-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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