K820125Substantially Equivalent

Cobe Centry 2000 Rx

Name: K820125 Cobe Centry 2000 Rx
Creator: Cobe Laboratories, Inc.
Published: 1982-03-23
License: https://open.fda.gov/license/

Cobe Laboratories, Inc., Mchenry IL / Traditional, Substantially Equivalent

FDA source

K820125 is the FDA 510(k) clearance record for COBE CENTRY 2000 RX, cleared for Cobe Laboratories, Inc. on 1982-03-23. FDA records list 77 510(k) clearances for Cobe Laboratories, Inc., from 1976-09-17 to 1993-05-11. As of 2026-09-10, FDA records show no recalls naming K820125.

Clearance record

Decision date: 1982-03-23
Received: 1982-01-18 (64 days to decision)
Review panel: Unknown
Applicant: Cobe Laboratories, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review: No