Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Laboratoire Ccd C/O Washington Regulatory Services · 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) |
|---|---|---|---|---|---|
| K890706 | CYTOBRUSH | Laboratoire Ccd C/O Washington Regulatory Services | 1989-04-25 | 74 | 0 |
| K884696 | RESUBMITTED ARTIFICIAL INSEMINATION INSTRUMENT SET | Laboratoire Ccd C/O Washington Regulatory Services | 1989-01-27 | 79 | 0 |
| K881456 | PIPELLE DE CORNIER ENDOMETRIAL SUCTION CURETTE | Laboratoire Ccd C/O Washington Regulatory Services | 1988-10-14 | 191 | 0 |
| K881220 | ENDOCYTE, DISPOSABLE ENDOMETRIAL SAMPLER | Laboratoire Ccd C/O Washington Regulatory Services | 1988-06-14 | 84 | 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