The following data is part of a premarket notification filed by Acro Biotech Llc. with the FDA for Acro Rapid Phencyclidine Urine Test, Catalog Pcp001000.
Device ID | K060353 |
510k Number | K060353 |
Device Name: | ACRO RAPID PHENCYCLIDINE URINE TEST, CATALOG PCP001000 |
Classification | Enzyme Immunoassay, Phencyclidine |
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 | LCM |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-02-13 |
Decision Date | 2006-05-03 |