510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K002447Substantially Equivalent

Modification to Rapid Drug Screen 9-Panel

American Bio Medica Corp., Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K002447 is the FDA 510(k) clearance record for MODIFICATION TO RAPID DRUG SCREEN 9-PANEL, a class II device, cleared for American Bio Medica Corp. on under FDA product code DKZ (Enzyme Immunoassay, Amphetamine). FDA records list 30 510(k) clearances for American Bio Medica Corp., from to . As of , FDA records show no recalls naming K002447.

Clearance record

Decision date
Received
(99 days to decision)
Product code
DKZ Enzyme Immunoassay, Amphetamine
Regulation
21 CFR 862.3100
Device class
Class II
Review panel
Clinical Toxicology
Applicant
American Bio Medica Corp. 1001 G St., NW, Washington DC
510(k) summary
Summary
Third party review
No

Clearances, product code DKZ

Trailing 12 months

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

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