CEPTI-SEAL DRESSING CHANGE KIT FOR VENOUS CATHETER— 510(k) K921347

Name: FDA 510(k) clearance K921347
Creator: U.S. Food and Drug Administration
Published: 1993-01-08

Unknown

Medi-Flex Hospital Products, Inc.

FDA 510(k) clearance K921347 for CEPTI-SEAL DRESSING CHANGE KIT FOR VENOUS CATHETER, Unknown on 1993-01-08. Applicant: Medi-Flex Hospital Products, Inc.. Device class: 2.

Clearance details

Applicant: Medi-Flex Hospital Products, Inc.
Product code: Code MCY
Device class: Class 2
Regulation: 21 CFR 880.5075
Advisory panel: General Hospital
Date received: 1992-03-18
Decision date: 1993-01-08
Decision: Unknown
Clearance type: Traditional
Location: Overland Park, KS, US

Download summary PDF View on FDA.gov ↗

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