510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K993852Substantially Equivalent

First Check Home Drug Test Panel 4

Worldwide Medical Corp., Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K993852 is the FDA 510(k) clearance record for FIRST CHECK HOME DRUG TEST PANEL 4, a class II device, cleared for Worldwide Medical Corp. on under FDA product code LAF (Gas Chromatography, Methamphetamine). FDA records list 9 510(k) clearances for Worldwide Medical Corp., from to . As of , FDA records show no recalls naming K993852.

Clearance record

Decision date
Received
(383 days to decision)
Product code
LAF Gas Chromatography, Methamphetamine
Regulation
21 CFR 862.3610
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Worldwide Medical Corp. 1900 K St. NW, Washington DC
510(k) summary
Summary
Third party review
No

Clearances, product code LAF

Trailing 12 months

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

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