The following data is part of a premarket notification filed by Sun Biomedical Laboratories, Inc. with the FDA for Visualine Ii Benzodiazepines.
Device ID | K953105 |
510k Number | K953105 |
Device Name: | VISUALINE II BENZODIAZEPINES |
Classification | Enzyme Immunoassay, Benzodiazepine |
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 | JXM |
CFR Regulation Number | 862.3170 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-07-03 |
Decision Date | 1995-10-05 |