The following data is part of a premarket notification filed by Solarcare Technologies Corp,inc. with the FDA for Stc Diagnostics Auto-lyte Urinary Hemoglobin Assay.
Device ID | K954326 |
510k Number | K954326 |
Device Name: | STC DIAGNOSTICS AUTO-LYTE URINARY HEMOGLOBIN ASSAY |
Classification | Calibrator, Secondary |
Applicant | SOLARCARE TECHNOLOGIES CORP,INC. 1745 EATON AVE. Bethlehem, PA 18018 -1799 |
Contact | R. Sam Niedbala |
Correspondent | R. Sam Niedbala SOLARCARE TECHNOLOGIES CORP,INC. 1745 EATON AVE. Bethlehem, PA 18018 -1799 |
Product Code | JIT |
CFR Regulation Number | 862.1150 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-09-15 |
Decision Date | 1996-07-23 |