Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Chongqing Peninsula Medical Technology Co., Ltd. · Predicate Candidate Screening
4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K192642 | 308nm Excimer System | Chongqing Peninsula Medical Technology Co., Ltd. | 2020-05-13 | 232 | 0 |
| K192552 | Irradiation Cosmetic Device | Chongqing Peninsula Medical Technology Co., Ltd. | 2020-04-17 | 213 | 0 |
| K172273 | 308nm Excimer System | Chongqing Peninsula Medical Technology Co., Ltd. | 2018-07-30 | 367 | 0 |
| K171835 | Irradiation Aesthetic Device | Chongqing Peninsula Medical Technology Co., Ltd. | 2018-01-30 | 224 | 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