The following data is part of a premarket notification filed by Tech-co, Inc. with the FDA for Creatine Kinase (colorimetric Method).
Device ID | K880178 |
510k Number | K880178 |
Device Name: | CREATINE KINASE (COLORIMETRIC METHOD) |
Classification | Colorimetric Method, Cpk Or Isoenzymes |
Applicant | TECH-CO, INC. 24111 BEVERLY Oak Park, MI 48237 |
Contact | Happy Chen |
Correspondent | Happy Chen TECH-CO, INC. 24111 BEVERLY Oak Park, MI 48237 |
Product Code | JHY |
CFR Regulation Number | 862.1215 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-01-15 |
Decision Date | 1988-02-18 |