The following data is part of a premarket notification filed by Solarcare Technologies Corp,inc. with the FDA for Microplate Cannabinoids Assay.
Device ID | K924815 |
510k Number | K924815 |
Device Name: | MICROPLATE CANNABINOIDS ASSAY |
Classification | Enzyme Immunoassay, Cannabinoids |
Applicant | SOLARCARE TECHNOLOGIES CORP,INC. 1745 EATON AVE. Bethlehem, PA 18018 -1799 |
Contact | Sam Niedbala |
Correspondent | Sam Niedbala SOLARCARE TECHNOLOGIES CORP,INC. 1745 EATON AVE. Bethlehem, PA 18018 -1799 |
Product Code | LDJ |
CFR Regulation Number | 862.3870 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-09-25 |
Decision Date | 1993-01-26 |