510(k) K232772 ยท DXQ Blood Pressure Cuff
Blood Pressure Cuff (1201D1,12L2D1,1202D1,12L3D1,1203D1,1204D1,1205D1,1206D1,1207D1-1#,1207D1-2#,1207D1-3#,1207D1-4#,1207D1-5#,1201B1,12L2B1,1202B1,12L3B1,1203B1,1204B1,1205B1,1206B1,1207B1-1#,1207B1-2#,,1207B1-3#,1207B1-4#,1207B1-5#,1201W2,12L2W2,1202W2,12L3W2,1203W2,1204W2,1205W2,1206W2 and 1207W2
| Applicant | Shenzhen Plinma Technology Co. , Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Nov 29, 2023 |
| Received | Sep 11, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232772
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.