Atlas FDA

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-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K840823TREONIC C30Vickers America Medical Corp.1984-03-23280
K831838LABORATORY DATA MGMT SYSTEM SDMSVickers America Medical Corp.1984-01-242310
K830748RESUSCITAIREVickers America Medical Corp.1983-06-221050
K830936TREONIC IP5Vickers America Medical Corp.1983-04-12190
K813239OXYGENAIRE NURING INCUBATORVickers America Medical Corp.1982-01-28720
K813238NEOCARE BABY-CONTROLLED INCUBATORVickers America Medical Corp.1982-01-22660
K811865VMA PEDIATRIC APNEA MATTRESSVickers America Medical Corp.1981-07-31300
K810792NEOCARE TEMPERATURE MONITORVickers America Medical Corp.1981-04-29370
K810571NEOCARE OXYGEN MONITORVickers America Medical Corp.1981-03-1180
K810067140 NEOCARE AIR CONTROLLED INCUBATORVickers America Medical Corp.1981-03-11570
K802251SP 120 SOPHISTICATEVickers America Medical Corp.1980-10-23370
K801246OXFORD HUMAN MILK PASTEURISERVickers America Medical Corp.1980-10-031280
K791645VICKERS MEDICAL MODEL 112 TREONIC DC2Vickers America Medical Corp.1979-10-02400
K791713VICKERS MEDICAL MODEL 130 NEAVENT-NEOVickers America Medical Corp.1979-09-19230
K790936MODEL 114 TREONIC H150 HAEMOHEATERVickers America Medical Corp.1979-09-041090
K790658AIRCRAFT TRANSIT ISOLATOR MODEL 121Vickers America Medical Corp.1979-07-03890
K790657STRETCHER TRANSIT ISOLATER #122Vickers America Medical Corp.1979-07-03890
K790945MODEL 113 TREONIC IP3 DIGITAL SYRINGE PUVickers America Medical Corp.1979-06-01140
K790689REVISED BATTERY CHARGERVickers America Medical Corp.1979-05-29490
K781562HEMACHECKVickers America Medical Corp.1978-11-15650
K781332PEEP/CPAP VALVEVickers America Medical Corp.1978-10-04630
K781325MARKII VENTIMASKSVickers America Medical Corp.1978-09-27570

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