Skip to content

Amikacin Reagent Test Kit

by Beckman Instruments, Inc. 510(k)

Active United States

510(k) K840647

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK840647 Date2 Apr 1984ClearedStatusActive

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  • Withdrawn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
LDN
Device Class
Class II
Regulation
21 CFR Part 862.3035
Advisory Committee
Clinical Toxicology
FDA Decision
SESE Substantially Equivalent

Other devices from Beckman Instruments, Inc.

See all devices from Beckman Instruments, Inc. →