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Modification to: Premier Platinum Hpsa

by Meridian Diagnostics, Inc.

510(k) K983255

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 NumberK983255 Date17 Dec 1998ClearedStatusActive

Recalls

1 recall · FDA

    • Terminated Z-0465-03 FDA Unclassified (pre-2012) initiated 26 Dec 2002

    Due to defective packaging, the firm cannot assure product stability through the labeled expiration date.

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  • Withdrawn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
LYR
Device Class
Class I
Regulation
21 CFR Part 866.3110
Advisory Committee
Microbiology
FDA Decision
SESE Substantially Equivalent

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