Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Vickers America Medical Corp. · Predicate Candidate Screening
22 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
57 daysmedian FDA review time
109 days90th percentile
22clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K840823 | TREONIC C30 | Vickers America Medical Corp. | 1984-03-23 | 28 | 0 |
| K831838 | LABORATORY DATA MGMT SYSTEM SDMS | Vickers America Medical Corp. | 1984-01-24 | 231 | 0 |
| K830748 | RESUSCITAIRE | Vickers America Medical Corp. | 1983-06-22 | 105 | 0 |
| K830936 | TREONIC IP5 | Vickers America Medical Corp. | 1983-04-12 | 19 | 0 |
| K813239 | OXYGENAIRE NURING INCUBATOR | Vickers America Medical Corp. | 1982-01-28 | 72 | 0 |
| K813238 | NEOCARE BABY-CONTROLLED INCUBATOR | Vickers America Medical Corp. | 1982-01-22 | 66 | 0 |
| K811865 | VMA PEDIATRIC APNEA MATTRESS | Vickers America Medical Corp. | 1981-07-31 | 30 | 0 |
| K810792 | NEOCARE TEMPERATURE MONITOR | Vickers America Medical Corp. | 1981-04-29 | 37 | 0 |
| K810571 | NEOCARE OXYGEN MONITOR | Vickers America Medical Corp. | 1981-03-11 | 8 | 0 |
| K810067 | 140 NEOCARE AIR CONTROLLED INCUBATOR | Vickers America Medical Corp. | 1981-03-11 | 57 | 0 |
| K802251 | SP 120 SOPHISTICATE | Vickers America Medical Corp. | 1980-10-23 | 37 | 0 |
| K801246 | OXFORD HUMAN MILK PASTEURISER | Vickers America Medical Corp. | 1980-10-03 | 128 | 0 |
| K791645 | VICKERS MEDICAL MODEL 112 TREONIC DC2 | Vickers America Medical Corp. | 1979-10-02 | 40 | 0 |
| K791713 | VICKERS MEDICAL MODEL 130 NEAVENT-NEO | Vickers America Medical Corp. | 1979-09-19 | 23 | 0 |
| K790936 | MODEL 114 TREONIC H150 HAEMOHEATER | Vickers America Medical Corp. | 1979-09-04 | 109 | 0 |
| K790658 | AIRCRAFT TRANSIT ISOLATOR MODEL 121 | Vickers America Medical Corp. | 1979-07-03 | 89 | 0 |
| K790657 | STRETCHER TRANSIT ISOLATER #122 | Vickers America Medical Corp. | 1979-07-03 | 89 | 0 |
| K790945 | MODEL 113 TREONIC IP3 DIGITAL SYRINGE PU | Vickers America Medical Corp. | 1979-06-01 | 14 | 0 |
| K790689 | REVISED BATTERY CHARGER | Vickers America Medical Corp. | 1979-05-29 | 49 | 0 |
| K781562 | HEMACHECK | Vickers America Medical Corp. | 1978-11-15 | 65 | 0 |
| K781332 | PEEP/CPAP VALVE | Vickers America Medical Corp. | 1978-10-04 | 63 | 0 |
| K781325 | MARKII VENTIMASKS | Vickers America Medical Corp. | 1978-09-27 | 57 | 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