Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Buffalo Medical Specialties Mfg., Inc. · 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) |
|---|---|---|---|---|---|
| K902132 | CUFF, BLOOD PRESSURE | Buffalo Medical Specialties Mfg., Inc. | 1990-06-29 | 50 | 0 |
| K852051 | EXTERNAL MALE CATHETER | Buffalo Medical Specialties Mfg., Inc. | 1985-08-22 | 105 | 0 |
| K830569 | CYNOX I HEMOGLOBINOMETER | Buffalo Medical Specialties Mfg., Inc. | 1983-04-08 | 45 | 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