The following data is part of a premarket notification filed by Sun Biomedical Laboratories, Inc. with the FDA for Visualine Ii Methamphetimine.
Device ID | K972032 |
510k Number | K972032 |
Device Name: | VISUALINE II METHAMPHETIMINE |
Classification | Enzyme Immunoassay, Amphetamine |
Applicant | SUN BIOMEDICAL LABORATORIES, INC. 2040 FAIRFAX AVE. Cherry Hill, NJ 08003 |
Contact | Ming Sun |
Correspondent | Ming Sun SUN BIOMEDICAL LABORATORIES, INC. 2040 FAIRFAX AVE. Cherry Hill, NJ 08003 |
Product Code | DKZ |
CFR Regulation Number | 862.3100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-06-02 |
Decision Date | 1997-08-12 |