510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K820187Substantially Equivalent

Syva Advance Sys. Emit,(r)-Aed(r) Pheny

Syva Co., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K820187 is the FDA 510(k) clearance record for SYVA ADVANCE SYS. EMIT,(R)-AED(R) PHENY, a class II device, cleared for Syva Co. on under FDA product code LES (Fluorescent Immunoassay, Diphenylhydantoin). FDA records list 212 510(k) clearances for Syva Co., from to . As of , FDA records show no recalls naming K820187.

Clearance record

Decision date
Received
(18 days to decision)
Product code
LES Fluorescent Immunoassay, Diphenylhydantoin
Regulation
21 CFR 862.3350
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Syva Co. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code LES

Trailing 12 months

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

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