Skip to content

Beckman Transferrin Kit

by Beckman Instruments, Inc. 510(k)

Active United States

510(k) K926272

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK926272 Date7 Oct 1993ClearedStatusActive

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  • Withdrawn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 22 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
DDG
Device Class
Class II
Regulation
21 CFR Part 866.5880
Advisory Committee
Immunology
FDA Decision
SESE Substantially Equivalent

Other devices from Beckman Instruments, Inc.

See all devices from Beckman Instruments, Inc. →