Medisign MM1000 BT Blood Glucose Monitoring System, Medisign MM1100 BT Blood Glucose Monitoring System, Medisign MM1200 BT Blood Glucose Monitoring System, Smart Diabetes Bluetooth Blood Glucose Monitoring System, Medisign MM 1000 BT MULTI Blood Glucose Monitoring System, Medisign MM 1100 BT MULTI Blood Glucose Monitoring System, Medisign MM 1200 BT MULTI Blood Glucose Monitoring System, Smart Diabetes Bluetooth Pro Blood Glucose Monitoring System
K152534 is the FDA 510(k) clearance record for Medisign MM1000 BT Blood Glucose Monitoring System, Medisign MM1100 BT Blood Glucose Monitoring System, Medisign MM1200 BT Blood Glucose Monitoring System, Smart Diabetes Bluetooth Blood Glucose Monitoring System, Medisign MM 1000 BT MULTI Blood Glucose Monitoring System, Medisign MM 1100 BT MULTI Blood Glucose Monitoring System, Medisign MM 1200 BT MULTI Blood Glucose Monitoring System, Smart Diabetes Bluetooth Pro Blood Glucose Monitoring System, a class II device, cleared for Tianjin Empecs Medical Device Co., Ltd. on under FDA product code NBW (System, Test, Blood Glucose, Over The Counter). FDA records list 4 510(k) clearances for Tianjin Empecs Medical Device Co., Ltd., from to . As of , FDA records show no recalls naming K152534.
Clearance record
- Decision date
- Received
- (564 days to decision)
- Product code
- NBW System, Test, Blood Glucose, Over The Counter
- Regulation
- 21 CFR 862.1345
- Device class
- Class II
- Review panel
- Clinical Chemistry
- Applicant
- Tianjin Empecs Medical Device Co., Ltd. # 35 And 37, Yingcheng St., Hangu, CN
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code NBW
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 1 |
| August 2026 | 1 |
| September 2026 | 0 |
| October 2026 | 0 |
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