The following data is part of a premarket notification filed by Teco Diagnostics with the FDA for Uritek Tc-101 Urine Analyzer, Urine Reagent Strips 10, Models Tc-101, Urs-10.
Device ID | K101673 |
510k Number | K101673 |
Device Name: | URITEK TC-101 URINE ANALYZER, URINE REAGENT STRIPS 10, MODELS TC-101, URS-10 |
Classification | Method, Enzymatic, Glucose (urinary, Non-quantitative) |
Applicant | TECO DIAGNOSTICS 1268 NORTH LAKEVIEW AVE. Anaheim, CA 92807 |
Contact | Kc Chen |
Correspondent | Kc Chen TECO DIAGNOSTICS 1268 NORTH LAKEVIEW AVE. Anaheim, CA 92807 |
Product Code | JIL |
Subsequent Product Code | CDM |
Subsequent Product Code | CEN |
Subsequent Product Code | JIN |
Subsequent Product Code | JIO |
Subsequent Product Code | JIR |
Subsequent Product Code | JJB |
Subsequent Product Code | JMT |
Subsequent Product Code | JRE |
Subsequent Product Code | KQO |
Subsequent Product Code | LJX |
CFR Regulation Number | 862.1340 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-06-15 |
Decision Date | 2011-02-04 |
Summary: | summary |