COBE CENTRY 2000 RX— 510(k) K820125

Substantially Equivalent

Cobe Laboratories, Inc.

FDA 510(k) clearance K820125 for COBE CENTRY 2000 RX, Substantially Equivalent on 1982-03-23. Applicant: Cobe Laboratories, Inc..

Clearance details

Applicant: Cobe Laboratories, Inc.
Advisory panel: Unknown
Date received: 1982-01-18
Decision date: 1982-03-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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