The following data is part of a premarket notification filed by Acro Biotech Llc. with the FDA for Acro Biotech Llc Rapid Benzoylecgonine Urine Test; Catalog# Met001000.
Device ID | K053035 |
510k Number | K053035 |
Device Name: | ACRO BIOTECH LLC RAPID BENZOYLECGONINE URINE TEST; CATALOG# MET001000 |
Classification | Enzyme Immunoassay, Cocaine And Cocaine Metabolites |
Applicant | ACRO BIOTECH LLC. 9500 7TH STREET UNIT M Rancho Cucamonga, CA 91730 -9094 |
Contact | Gregory Lee |
Correspondent | Gregory Lee ACRO BIOTECH LLC. 9500 7TH STREET UNIT M Rancho Cucamonga, CA 91730 -9094 |
Product Code | DIO |
CFR Regulation Number | 862.3250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-10-27 |
Decision Date | 2006-05-05 |