Acon Laboratories Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Acon Laboratories Co. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Acon Laboratories Co. has 6 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 6 cleared submissions from 1998 to 2009. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Acon Laboratories Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Acon Laboratories Co.
6 devices
Cleared
Apr 08, 2009
ON-CALL PLUS BLOOD GLUCOSE MONITORING SYSTEM
Chemistry
90d
Cleared
Aug 11, 2006
ACON URINALYSIS REAGENT STRIPS
Chemistry
67d
Cleared
Feb 10, 2003
ACON STREP A TWIST TEST DEVICE
Microbiology
90d
Cleared
May 08, 2002
ACON ONE STEP MULTI-DRUG MULTI-LINE SCREEN TEST CARD
Toxicology
98d
Cleared
May 07, 2001
ACON STREP A RAPID TEST STRIP
Microbiology
69d
Cleared
Apr 16, 1998
ACON HCG ONE STEP URINE/SERUM PREGNANCY TEST
Chemistry
50d