The following data is part of a premarket notification filed by Syntron Bioresearch, Inc. with the FDA for Quikstrip One Step Phencyclidine (pcp) Test.
Device ID | K981019 |
510k Number | K981019 |
Device Name: | QUIKSTRIP ONE STEP PHENCYCLIDINE (PCP) TEST |
Classification | Enzyme Immunoassay, Phencyclidine |
Applicant | SYNTRON BIORESEARCH, INC. 1420 LOS ANGELES AVE. SUITE 201 Simi Valley, CA 93065 |
Contact | Cleve W Laird |
Correspondent | Cleve W Laird SYNTRON BIORESEARCH, INC. 1420 LOS ANGELES AVE. SUITE 201 Simi Valley, CA 93065 |
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 | 1998-03-18 |
Decision Date | 1998-05-07 |
Summary: | summary |