Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K862419Substantially Equivalent

Serum Vancomycin Toxicology Control

Utak Laboratories Inc, Canyon Country CA / Traditional, Substantially Equivalent

K862419 is the FDA 510(k) clearance record for SERUM VANCOMYCIN TOXICOLOGY CONTROL, a class I device, cleared for Utak Laboratories, Inc. on under FDA product code LAS (Drug Specific Control Materials). FDA records list 23 510(k) clearances for Utak Laboratories, Inc., from to . As of , FDA records show no recalls naming K862419.

Clearance record

Decision date
Received
(141 days to decision)
Product code
LAS Drug Specific Control Materials
Regulation
21 CFR 862.3280
Device class
Class I
Review panel
Clinical Toxicology
Applicant
Utak Laboratories, Inc. 26752 Oak Ave. # 5, Canyon Country CA
Third party review
No

Clearances, product code LAS

Trailing 12 months

FDA records hold no clearances under product code LAS in the trailing twelve months.

FDA records show no clearances under product code LAS in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LAS, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260