Skip to content

Enzygnost Platelet Factor 4 (PF4) Kit

by Behring Diagnostics, Inc. 510(k)

Active United States

510(k) K890633

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK890633 Date21 Apr 1989ClearedStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 11 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
LCO
Device Class
Class II
Regulation
21 CFR Part 864.7695
Advisory Committee
Hematology
FDA Decision
SESE Substantially Equivalent

Other devices from Behring Diagnostics, Inc.

See all devices from Behring Diagnostics, Inc. →