The following data is part of a premarket notification filed by Mesure Technology Co.,ltd. with the FDA for Digital Clinical Thermometer/models St8c Series.
Device ID | K071019 |
510k Number | K071019 |
Device Name: | DIGITAL CLINICAL THERMOMETER/MODELS ST8C SERIES |
Classification | Thermometer, Electronic, Clinical |
Applicant | MESURE TECHNOLOGY CO.,LTD. 7F, 88, SEC. 1, KWANG FU ROAD SAN CHUNG CITY Taipei Hsien, TW R.o.c. |
Contact | John Chen |
Correspondent | John Chen MESURE TECHNOLOGY CO.,LTD. 7F, 88, SEC. 1, KWANG FU ROAD SAN CHUNG CITY Taipei Hsien, TW R.o.c. |
Product Code | FLL |
CFR Regulation Number | 880.2910 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2007-04-10 |
Decision Date | 2007-04-27 |