Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K791979Substantially Equivalent

Technicon Fast-Lc Sys. Anticonvu Drugs

Technicon Instruments Corp., Walker MI / Traditional, Substantially Equivalent

K791979 is the FDA 510(k) clearance record for TECHNICON FAST-LC SYS. ANTICONVU DRUGS, a class II device, cleared for Technicon Instruments Corp. on under FDA product code DPE (Thin Layer Chromatography, Diphenylhydantoin). FDA records list 157 510(k) clearances for Technicon Instruments Corp., from to . As of , FDA records show no recalls naming K791979.

Clearance record

Decision date
Received
(49 days to decision)
Product code
DPE Thin Layer Chromatography, Diphenylhydantoin
Regulation
21 CFR 862.3350
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Technicon Instruments Corp. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code DPE

Trailing 12 months

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

FDA records show no clearances under product code DPE in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DPE, 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