Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Medic-Aid , Ltd. — Predicate Candidate Screening
9 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
91 daysmedian FDA review time
294 days90th percentile
9clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K991685 | HALOLITE AAD SYSTEM WITH DEDICATED COMPRESSOR | Medic-Aid , Ltd. | 1999-08-13 | 88 | 0 |
| K981772 | HALOLITE AAD SYSTEM | Medic-Aid , Ltd. | 1998-11-03 | 168 | 0 |
| K971933 | PORT-NEB | Medic-Aid , Ltd. | 1997-08-01 | 66 | 0 |
| K934749 | FREEWAY LITE NEBULIZER COMPRESSOR | Medic-Aid , Ltd. | 1994-07-25 | 294 | 0 |
| K940887 | SYSTEM 22 ADULT MASK | Medic-Aid , Ltd. | 1994-04-19 | 53 | 0 |
| K940888 | SYSTEM 22 PAEDIATRIC MASK | Medic-Aid , Ltd. | 1994-04-19 | 53 | 0 |
| K933535 | VENTSTREAM DRUG NEBULIZER | Medic-Aid , Ltd. | 1994-01-24 | 187 | 0 |
| K924123 | SIDESTREAM DISPOSABLE | Medic-Aid , Ltd. | 1992-11-16 | 91 | 0 |
| K914152 | SIDESTREAM DRUG NEBULIZER | Medic-Aid , Ltd. | 1992-05-05 | 232 | 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