Acro Biotech, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Acro Biotech, LLC - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Acro Biotech, LLC has 8 FDA 510(k) cleared medical devices. Based in Rancho Cucamonga, US.
Historical record: 8 cleared submissions from 2006 to 2006. Primary specialty: Toxicology.
Browse the FDA 510(k) cleared devices submitted by Acro Biotech, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Acro Biotech, LLC
8 devices
Cleared
Aug 07, 2006
ACRO BIOTECH LLC RAPID MDMA URINE TEST, CATALOG MDMA0010000
Toxicology
175d
Cleared
Jul 28, 2006
ACRO BIOTECH LLC RAPID BENZODIAZEPINE URINE TEST, CATALOG BZD001000
Toxicology
165d
Cleared
Jun 15, 2006
ACRO BIOTECH LLC RAPID OPIATES URINE TEST
Toxicology
231d
Cleared
Jun 06, 2006
ACRO BIOTECH LLC RAPID METHAMPHETAMINE URINE TEST
Chemistry
222d
Cleared
Jun 06, 2006
ACRO BIOTECH LLC RAPID TETRAHYDROCANNABINOL URINE TEST
Toxicology
222d
Cleared
May 05, 2006
ACRO BIOTECH LLC RAPID BENZOYLECGONINE URINE TEST
Toxicology
190d
Cleared
May 03, 2006
ACRO RAPID PHENCYCLIDINE URINE TEST, CATALOG PCP001000
Toxicology
79d
Cleared
Feb 09, 2006
ACRO BIOTECH LLC RAPID AMPHETAMINE URINE TEST
Toxicology
105d