Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Prolax Medical Products, 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) |
|---|---|---|---|---|---|
| K903351 | PROLAX DISPOSABLE LATEX GLOVES (PROCEDURE STERILE) | Prolax Medical Products, Inc. | 1990-09-26 | 62 | 0 |
| K903350 | PROLAX DISPOSABLE LATEX GLOVES (EXAM) HYPOALLERGEN | Prolax Medical Products, Inc. | 1990-08-23 | 29 | 0 |
| K903352 | PROLAX DISPOSABLE LATEX GLOVES (EXAMINATION) | Prolax Medical Products, Inc. | 1990-08-23 | 28 | 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