Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Shenzhen Jamr Technology Co., Ltd. · Predicate Candidate Screening
7 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
180 daysmedian FDA review time
210 days90th percentile
7clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K253570 | Blood Pressure Monitor (W06LT) | Shenzhen Jamr Technology Co., Ltd. | 2026-05-20 | 184 | 0 |
| K251331 | Blood Pressure Monitor (B73, BE23T) | Shenzhen Jamr Technology Co., Ltd. | 2025-10-27 | 180 | 0 |
| K233823 | Ultrasonic Fetal Doppler | Shenzhen Jamr Technology Co., Ltd. | 2024-06-28 | 210 | 0 |
| K233146 | Blood Pressure Monitor | Shenzhen Jamr Technology Co., Ltd. | 2024-03-19 | 174 | 0 |
| K230409 | Wrist Type Blood Pressure Monitor (W05,W1101L) | Shenzhen Jamr Technology Co., Ltd. | 2023-08-25 | 191 | 0 |
| K220886 | Upper Arm Type Blood Pressure Monitor | Shenzhen Jamr Technology Co., Ltd. | 2022-07-27 | 121 | 0 |
| K200437 | Blood Pressure Monitor | Shenzhen Jamr Technology Co., Ltd. | 2020-06-25 | 122 | 0 |
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