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Psa Antibody Kit

by Ventana Medical Systems, Inc. 2 variants

510(k) K932326

Psa Antibody Kit is a Class II device made by Ventana Medical Systems, Inc., cleared under FDA 510(k) K932326 on 6 Aug 1993, active as of 11 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 11 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 11 Oct 2026.

Regulatory status

as of registry sync 11 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK932326 Date6 Aug 1993ClearedStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
DEH
Device class
Class II
Regulation
21 CFR Part 866.5550
Advisory committee
Immunology
FDA decision
SESE Substantially Equivalent

Similar devices

Other devices filed under FDA product code DEH (Lambda, Antigen, Antiserum, Control).

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