Joytech Healthcare Co. , Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 21
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K252685 | Arm-type Fully Automatic Digital Blood Pressure Monitor (DBP-61D2L, DBP-61D2L-P, DBP-63D2L, DBP-63D2 | February 13, 2026 |
| K243468 | Compressor Nebulizer (NB-1100); Compressor Nebulizer (NB-1101); Compressor Nebulizer (NB-1102); Comp | July 2, 2025 |
| K250548 | Arm-type Fully Automatic Digital Blood Pressure Monitors (DBP-6286B, DBP-6186) | June 26, 2025 |
| K241431 | Arm-type Fully Automatic Digital Blood Pressure Monitor (DBP-62D0L, DBP-62D0B, DBP-61D0, DBP-61D0L, | January 13, 2025 |
| K241322 | Electric Breast Pump (LD-208L, LD-3010L, LD-2010L, LD-3010, LD-2010) | December 19, 2024 |
| K231303 | Arm-type Fully Automatic Digital Blood Pressure Monitor | January 26, 2024 |
| K230566 | Arm-type Fully Automatic Digital Blood Pressure Monitor, Wrist-type Fully Automatic Digital Blood Pr | August 25, 2023 |
| K213189 | Wrist-type Fully Automatic Digital Blood Pressure Monitor | March 1, 2022 |
| K212115 | Arm-type Fully Automatic Digital Blood Pressure Monitor, Wrist-type Fully Automatic Digital Blood Pr | January 5, 2022 |
| K200649 | Arm-Type Fully Automatic Digital Blood Pressure Monitor | August 3, 2020 |
| K200599 | Digital Thermometer | July 8, 2020 |
| K183393 | Digital Thermometer | November 18, 2019 |
| K190886 | Non-invasive blood pressure measurement systems | July 29, 2019 |
| K190873 | Infrared Ear/Forehead Thermometer | July 26, 2019 |
| K182629 | Digital Thermometer | February 28, 2019 |
| K181239 | Infrared Forehead Thermometer, Infrared Ear/Forehead Thermometer | October 29, 2018 |
| K181081 | Infrared Ear Thermometer | October 2, 2018 |
| K173024 | Non-invasive blood pressure measurement systems | August 22, 2018 |
| K172989 | Electric Breast Pump | December 20, 2017 |
| K170666 | The Wrist-Type Fully Automatic Digital Blood Pressure Monitors | November 22, 2017 |