Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
The Boston & Pacific Co., Inc. · 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) |
|---|---|---|---|---|---|
| K896726 | 4 SURE EXTERNAL MALE CATHETER | The Boston & Pacific Co., Inc. | 1990-02-26 | 89 | 0 |
| K896727 | 4 SURE URINARY DRAIN BAG | The Boston & Pacific Co., Inc. | 1990-02-20 | 83 | 0 |
| K896728 | 4 SURE URINARY LEG BAG | The Boston & Pacific Co., Inc. | 1990-02-20 | 83 | 0 |
| K896725 | 4 SURE UROLOGICAL CATHETER | The Boston & Pacific Co., Inc. | 1990-02-16 | 79 | 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