Txit D.A.U. Barbiturate Assay (Modification)

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K920314 ↗

FDA Product Code

DIS

Device Class

Class II

Regulation

21 CFR Part 862.3150

Advisory Committee

Clinical Toxicology

FDA Decision

SESE Substantially Equivalent

• Surgipress Surgical Loop

  Class I

  FDA 510(k) K843593 Active Cleared 24 Oct 1984

• Fiber Optic Handpiece

  Class I

  FDA 510(k) K780483 Active Cleared 28 Apr 1978

• S-100 CT Scanner

  Class II

  FDA 510(k) K780769 Active Cleared 2 Jun 1978

• Hi-Sensitivity Mode Option for S60-1A

  Class II

  FDA 510(k) K761332 Active Cleared 30 Dec 1976

• Amalgam Alloy

  Class II

  FDA 510(k) K780997 Active Cleared 27 Jul 1978

• Syntex System 6000

  Class II

  FDA 510(k) K761330 Active Cleared 30 Dec 1976

See all devices from Syntex Corp. →