Skip to content

Aia-Pack Myoglobin Assay

by Tosoh Medics, Inc.

510(k) K981012

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

1 closed

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK981012 Date28 May 1998ClearedStatusActive

Recalls

1 recall · FDA

    • Terminated Z-2072-2018 FDA Class II initiated 5 Mar 2018

    Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which potentially causes falsely increased or falsely decreased immunoassay test results, depending upon the assay.

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  • Withdrawn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
DDR
Device Class
Class II
Regulation
21 CFR Part 866.5680
Advisory Committee
Immunology
FDA Decision
SESE Substantially Equivalent

Other devices from Tosoh Medics, Inc.

See all devices from Tosoh Medics, Inc. →