Atlas FDA

Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account

Shenzhen Jumper Medical Equipment Co., Ltd. · Predicate Candidate Screening

10 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

195 daysmedian FDA review time
293 days90th percentile
10clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K231310Electronic Blood Pressure MonitorShenzhen Jumper Medical Equipment Co., Ltd.2023-10-271750
K182871Mini TENS Therapy DeviceShenzhen Jumper Medical Equipment Co., Ltd.2019-08-012930
K182437Wireless Intelligent ThermometerShenzhen Jumper Medical Equipment Co., Ltd.2019-05-052400
K182495Electronic Blood Pressure MonitorShenzhen Jumper Medical Equipment Co., Ltd.2019-03-031730
K172795Infrared ThermometerShenzhen Jumper Medical Equipment Co., Ltd.2018-03-141800
K170965Fingertip Pulse OximeterShenzhen Jumper Medical Equipment Co., Ltd.2017-11-032170
K140582FINGERTIP PULSE OXIMETERShenzhen Jumper Medical Equipment Co., Ltd.2014-08-281750
K131457FETAL ULTRASONIC MONITOR AND ACCESSORIESShenzhen Jumper Medical Equipment Co., Ltd.2014-01-242490
K131243NON-CONTACT INFRARED THERMOMETERShenzhen Jumper Medical Equipment Co., Ltd.2013-11-121950
K110124FETAL DOPPLER JPD-100SShenzhen Jumper Medical Equipment Co., Ltd.2011-02-04170

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda