The following data is part of a premarket notification filed by Sun Biomedical Laboratories, Inc. with the FDA for Visualine Ii (also Known As Sunline) Phencyclidine.
Device ID | K983790 |
510k Number | K983790 |
Device Name: | VISUALINE II (ALSO KNOWN AS SUNLINE) PHENCYCLIDINE |
Classification | Enzyme Immunoassay, Phencyclidine |
Applicant | SUN BIOMEDICAL LABORATORIES, INC. 604 VPR CENTER 1001 LOWER LANDING RD. Blackwood, NJ 08012 |
Contact | Ming Sun |
Correspondent | Ming Sun SUN BIOMEDICAL LABORATORIES, INC. 604 VPR CENTER 1001 LOWER LANDING RD. Blackwood, NJ 08012 |
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 | 1998-10-27 |
Decision Date | 1999-03-01 |