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ADVIA® Chemistry TCA 10283014

by Siemens Healthcare Diagnostics Inc.

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00630414551036 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
ADVIA® Chemistry TCA
Generic Name
Tricyclic antidepressant IVD, kit, enzyme immunoassay (EIA)
Model / Ref / Catalog
10283014, 6520218
Description
Tricyclic Antidepressants - ADVIA Chem. - RGT - 4x100 tests
Primary DI / UDI-DI
00630414551036
510(k) Number
FDA Product Code
LFH
GMDN Term
Tricyclic antidepressant IVD, kit, enzyme immunoassay (EIA)
Device Class
Class II
Regulation Number
862.3910
GUDID distribution status
Not in Commercial Distribution

Related devices

Cleared under the same submission (K961393)

Other devices from Siemens Healthcare Diagnostics Inc.

See all devices from Siemens Healthcare Diagnostics Inc. →

Properties

  • Lot / Batch Number
  • Expiration Date

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No