510(k) K172972
K172972 is an FDA 510(k) premarket notification submitted by Shenzhen Jiacom Technology CO ., Ltd. for the device "Wrist Type Automatic Blood Pressure Monitor". The FDA issued a decision of Substantially Equivalent on Mar 2, 2018. The device falls under product code DXN (System, Measurement, Blood-Pressure, Non-Invasive), a Class II device regulated under 21 CFR 870.1130. Shenzhen Jiacom Technology CO ., Ltd. has 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Mar 2, 2018
- Date Received
- Sep 26, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Measurement, Blood-Pressure, Non-Invasive
- Device Class
- Class II
- Regulation Number
- 870.1130
- Review Panel
- CV
- Submission Type
- 510(k)