Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Medimop Medical Projects, Ltd. · Predicate Candidate Screening
12 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
71 daysmedian FDA review time
98 days90th percentile
12clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K160503 | Vented Vial Adapter Transfer Device - 13mm | Medimop Medical Projects, Ltd. | 2016-05-04 | 70 | 0 |
| K140730 | VIAL2BAG DIRECT CONNECT | Medimop Medical Projects, Ltd. | 2014-06-12 | 80 | 0 |
| K130179 | MP VIAL ADAPTER 13MM | Medimop Medical Projects, Ltd. | 2013-08-08 | 195 | 0 |
| K132040 | VIAL CONNECTOR 13MM CLOSED COLLAR | Medimop Medical Projects, Ltd. | 2013-07-31 | 29 | 0 |
| K122023 | MIXJECT WITH SPRAY HEAD | Medimop Medical Projects, Ltd. | 2012-10-04 | 85 | 0 |
| K072511 | SWABABLE VIAL ADAPTER 13MM, SWABABLE VIAL ADAPTER 20MM | Medimop Medical Projects, Ltd. | 2007-12-13 | 98 | 0 |
| K072759 | VIAL2BAG | Medimop Medical Projects, Ltd. | 2007-12-13 | 76 | 1 |
| K062482 | VENTED VIAL ADAPTER TRANSFER DEVICE | Medimop Medical Projects, Ltd. | 2006-11-03 | 71 | 0 |
| K031861 | MIX2VIAL TRANSFER DEVICE | Medimop Medical Projects, Ltd. | 2003-07-29 | 43 | 0 |
| K001831 | NEEDLELESS TRANSFER DEVICE | Medimop Medical Projects, Ltd. | 2000-07-11 | 25 | 0 |
| K001293 | MODIFICATION TO MIXJECT DISPENSING PIN/WITH DETACHABLE VIAL | Medimop Medical Projects, Ltd. | 2000-05-05 | 11 | 0 |
| K963583 | MIXJECT DISPENSING PIN/WITH DETACHABLE VIAL HOLDER/WITH DETA | Medimop Medical Projects, Ltd. | 1996-10-07 | 31 | 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