510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K803039Substantially Equivalent

Profile Anti-Convul. Set Assayed S. Ctl.

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

K803039 is the FDA 510(k) clearance record for PROFILE ANTI-CONVUL. SET ASSAYED S. CTL., a class I device, cleared for General Diagnostics on under FDA product code DIF (Drug Mixture Control Materials). FDA records list 39 510(k) clearances for General Diagnostics, from to . As of , FDA records show no recalls naming K803039.

Clearance record

Decision date
Received
(21 days to decision)
Product code
DIF Drug Mixture Control Materials
Regulation
21 CFR 862.3280
Device class
Class I
Review panel
Clinical Toxicology
Applicant
General Diagnostics 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code DIF

Trailing 12 months

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

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