Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Mem Medical, Inc. · Predicate Candidate Screening
27 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
12 daysmedian FDA review time
14 days90th percentile
27clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K791909 | IMV BUSHING #M-513 | Mem Medical, Inc. | 1979-10-09 | 14 | 0 |
| K791912 | IMV FOR MONITORING #M-510 | Mem Medical, Inc. | 1979-10-09 | 14 | 0 |
| K791905 | IMV W/BAG & TUBING #M-508 | Mem Medical, Inc. | 1979-10-09 | 14 | 0 |
| K791911 | FALL-SAFE IMV #M-511 | Mem Medical, Inc. | 1979-10-09 | 14 | 0 |
| K791907 | RETARD VALVE 3-STACK #M-515 | Mem Medical, Inc. | 1979-10-09 | 14 | 0 |
| K791910 | THREE LITER BAG #M-512 | Mem Medical, Inc. | 1979-10-09 | 14 | 0 |
| K791908 | RETARD VALVE 3-STACK #M-514 | Mem Medical, Inc. | 1979-10-09 | 14 | 0 |
| K791906 | IMV W/BAG #M-507 | Mem Medical, Inc. | 1979-10-09 | 14 | 0 |
| K791913 | IMV MANIFOLD #M-506 | Mem Medical, Inc. | 1979-10-09 | 14 | 0 |
| K791904 | IMV W/BAG & HOSES #M-509 | Mem Medical, Inc. | 1979-10-09 | 14 | 0 |
| K791849 | ONE-WAY VALVE-MALE, M-504 | Mem Medical, Inc. | 1979-10-01 | 12 | 0 |
| K791850 | ONE-WAY VALVE-FEMALE, M-503 | Mem Medical, Inc. | 1979-10-01 | 12 | 0 |
| K791853 | TEE- TWO-WAY VALVES M-500 | Mem Medical, Inc. | 1979-10-01 | 12 | 0 |
| K791852 | T-PC FOR R.F. M.D., M-501 | Mem Medical, Inc. | 1979-10-01 | 12 | 0 |
| K791851 | RED CAP, M-502 | Mem Medical, Inc. | 1979-10-01 | 12 | 0 |
| K791848 | RESPIROMETER MANIFOLD M-505 | Mem Medical, Inc. | 1979-10-01 | 12 | 0 |
| K790930 | TRACHE FITTING M-307 | Mem Medical, Inc. | 1979-06-22 | 38 | 0 |
| K790924 | NEBULIZER NO. M-175 | Mem Medical, Inc. | 1979-05-21 | 6 | 0 |
| K790927 | OXYGENERATOR NO. M-049 | Mem Medical, Inc. | 1979-05-21 | 6 | 0 |
| K790926 | NEBULIZER WITH MOUTHPIECE AND TEE | Mem Medical, Inc. | 1979-05-21 | 6 | 0 |
| K790933 | MOUTHPIECE M-187 | Mem Medical, Inc. | 1979-05-21 | 6 | 0 |
| K790931 | CORRUGATED TUBE WITH MOUTHPIECE | Mem Medical, Inc. | 1979-05-21 | 6 | 0 |
| K790929 | DRAINAGE BAG | Mem Medical, Inc. | 1979-05-21 | 6 | 0 |
| K790934 | OXYGEN BARB M-552 | Mem Medical, Inc. | 1979-05-21 | 6 | 0 |
| K790928 | 3-WAY T 22MM MALE | Mem Medical, Inc. | 1979-05-21 | 6 | 0 |
| K790925 | NEBULIZER WITH 4-WAY T NO M-174 | Mem Medical, Inc. | 1979-05-21 | 6 | 0 |
| K790932 | AEROSOL MOUTHPIECE NO. M-091 | Mem Medical, Inc. | 1979-05-21 | 6 | 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