Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Shenzhen Jiacom Technology CO ., Ltd. — Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K172874Infrared ThermometerShenzhen Jiacom Technology CO ., Ltd.2018-07-122940
K172894Infrared ThermometerShenzhen Jiacom Technology CO ., Ltd.2018-05-172370
K172972Wrist Type Automatic Blood Pressure MonitorShenzhen Jiacom Technology CO ., Ltd.2018-03-021570
K172896Arm Type Automatic Blood Pressure Monitor BP310A, BP313A, BPShenzhen Jiacom Technology CO ., Ltd.2018-01-261260

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