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-NumberDeviceDate
K252685Arm-type Fully Automatic Digital Blood Pressure Monitor (DBP-61D2L, DBP-61D2L-P, DBP-63D2L, DBP-63D2February 13, 2026
K243468Compressor Nebulizer (NB-1100); Compressor Nebulizer (NB-1101); Compressor Nebulizer (NB-1102); CompJuly 2, 2025
K250548Arm-type Fully Automatic Digital Blood Pressure Monitors (DBP-6286B, DBP-6186)June 26, 2025
K241431Arm-type Fully Automatic Digital Blood Pressure Monitor (DBP-62D0L, DBP-62D0B, DBP-61D0, DBP-61D0L, January 13, 2025
K241322Electric Breast Pump (LD-208L, LD-3010L, LD-2010L, LD-3010, LD-2010)December 19, 2024
K231303Arm-type Fully Automatic Digital Blood Pressure MonitorJanuary 26, 2024
K230566Arm-type Fully Automatic Digital Blood Pressure Monitor, Wrist-type Fully Automatic Digital Blood PrAugust 25, 2023
K213189Wrist-type Fully Automatic Digital Blood Pressure MonitorMarch 1, 2022
K212115Arm-type Fully Automatic Digital Blood Pressure Monitor, Wrist-type Fully Automatic Digital Blood PrJanuary 5, 2022
K200649Arm-Type Fully Automatic Digital Blood Pressure MonitorAugust 3, 2020
K200599Digital ThermometerJuly 8, 2020
K183393Digital ThermometerNovember 18, 2019
K190886Non-invasive blood pressure measurement systemsJuly 29, 2019
K190873Infrared Ear/Forehead ThermometerJuly 26, 2019
K182629Digital ThermometerFebruary 28, 2019
K181239Infrared Forehead Thermometer, Infrared Ear/Forehead ThermometerOctober 29, 2018
K181081Infrared Ear ThermometerOctober 2, 2018
K173024Non-invasive blood pressure measurement systemsAugust 22, 2018
K172989Electric Breast PumpDecember 20, 2017
K170666The Wrist-Type Fully Automatic Digital Blood Pressure MonitorsNovember 22, 2017