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TRANSPROBE-1

by Osi Pharmaceuticals, Inc.

PMA P880045

Withdrawn Withdrawn in United States.

Was authorized under PMA, withdrawn

Ended

Withdrawn 3 Oct 1989

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United StatesFDA PMAAPWD Approval withdrawn NumberP880045 Date3 Oct 1989Approval withdrawnStatusWithdrawn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  • Withdrawn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United States — FDA PMA Withdrawn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
Osi Transprobe-1
Generic Name
DNA-probe, human chromosome
PMA Number
FDA Product Code
MAO
Device Class
U
Advisory Committee
Pathology
FDA Decision
APWD Approval withdrawn