Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Medical Safety Products, Inc. · Predicate Candidate Screening
6 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
78 daysmedian FDA review time
85 days90th percentile
6clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K942624 | LOK-ON NEEDLE DISPOSAL CONTAINER | Medical Safety Products, Inc. | 1994-08-25 | 85 | 0 |
| K913329 | V-ACCI-GUARD(TM) REUSABLE HOLDER | Medical Safety Products, Inc. | 1991-08-23 | 29 | 0 |
| K895075 | ACCI-GUARD REUSABLE HOLDER | Medical Safety Products, Inc. | 1989-10-31 | 78 | 0 |
| K890751 | ACCI-GUARD(TM) I.V. CATHETER PLACEMENT UNIT | Medical Safety Products, Inc. | 1989-04-21 | 67 | 0 |
| K884139 | ACCI-GUARD(TM) REGULAR AND PEDIATRIC HOLDER | Medical Safety Products, Inc. | 1988-10-06 | 6 | 0 |
| K881654 | ACCI-GUARD MULTI-SAMPLE BLOOD COLLECTION NEEDLE | Medical Safety Products, Inc. | 1988-07-08 | 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