Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Shenzhen Kingboom Technology Co., Ltd. · Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K260473 | Electric nasal aspirator (BC027, BC030, BC033, BC035, BC035B | Shenzhen Kingboom Technology Co., Ltd. | 2026-05-12 | 89 | 0 |
| K260147 | Electric nasal aspirator (BC026, BC025, BC023, BC028, BC029, | Shenzhen Kingboom Technology Co., Ltd. | 2026-03-13 | 52 | 0 |
| K250697 | Electric Nasal Aspirator (BC026, BC025, BC023) | Shenzhen Kingboom Technology Co., Ltd. | 2025-04-23 | 47 | 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