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Cobe Centry TPE System

by Gambro Bct, Inc.

PMA P810023

Withdrawn Withdrawn in United States.

Was authorized under PMA, withdrawn

Ended

Withdrawn 16 Mar 1982

PMA

FDA recalls

None found

in data synced 6 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA PMA, synced 6 Oct 2026. What this means

Regulatory status

as of registry sync 6 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA PMAAPWD Approval withdrawn NumberP810023 Date16 Mar 1982Approval withdrawnStatusWithdrawn

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 6 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA PMA Withdrawn

Specification

PMA

Full name
Cobe Centry(R) Tpe System
Generic Name
Separator, automated, blood cell and plasma, therapeutic
PMA Number
FDA Product Code
LKN
Device Class
U
Advisory Committee
Gastroenterology, Urology
FDA Decision
APWD Approval withdrawn

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