COBE CENTRY 2 VARIABLE CONCENTRATE-18-— 510(k) K802895

Name: FDA 510(k) clearance K802895
Creator: U.S. Food and Drug Administration
Published: 1980-12-22

Substantially Equivalent

Cobe Laboratories, Inc.

FDA 510(k) clearance K802895 for COBE CENTRY 2 VARIABLE CONCENTRATE-18-, Substantially Equivalent on 1980-12-22. Applicant: Cobe Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Cobe Laboratories, Inc.
Product code: Code KDC
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1980-11-17
Decision date: 1980-12-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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