510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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Vickers America Medical Corp.

Mchenry, IL, US

Vickers America Medical Corp. appears in FDA device records in Mchenry, IL. FDA records list 22 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.

FDA records held for this company

510(k) clearances
22
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 22 510(k) clearances for Vickers America Medical Corp. between 1978 and 1984. The busiest year on record is 1979, with 7. The most recent is 1984, with 2.

Clearances by year, as a table
510(k) clearance decisions for Vickers America Medical Corp., by decision year
YearClearances
19783
19797
19802
19814
19822
19832
19842
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K840823TREONIC C30LDRSubstantially Equivalent
K831838LABORATORY DATA MGMT SYSTEM SDMSJQPSubstantially Equivalent
K830748RESUSCITAIREFMTSubstantially Equivalent
K830936TREONIC IP5FRNSubstantially Equivalent
K813239OXYGENAIRE NURING INCUBATORFMZSubstantially Equivalent
K813238NEOCARE BABY-CONTROLLED INCUBATORFMZSubstantially Equivalent
K811865VMA PEDIATRIC APNEA MATTRESSBZQSubstantially Equivalent
K810792NEOCARE TEMPERATURE MONITORFMZSubstantially Equivalent
K810571NEOCARE OXYGEN MONITORCCLSubstantially Equivalent
K810067140 NEOCARE AIR CONTROLLED INCUBATORFMZSubstantially Equivalent
K802251SP 120 SOPHISTICATEJQPSubstantially Equivalent
K801246OXFORD HUMAN MILK PASTEURISERHGXSubstantially Equivalent
K791645VICKERS MEDICAL MODEL 112 TREONIC DC2FKWSubstantially Equivalent
K791713VICKERS MEDICAL MODEL 130 NEAVENT-NEOCBKSubstantially Equivalent
K790936MODEL 114 TREONIC H150 HAEMOHEATERKZLSubstantially Equivalent
K790658AIRCRAFT TRANSIT ISOLATOR MODEL 121LGNSubstantially Equivalent
K790657STRETCHER TRANSIT ISOLATER #122LGMSubstantially Equivalent
K790945MODEL 113 TREONIC IP3 DIGITAL SYRINGE PUFRNSubstantially Equivalent
K790689REVISED BATTERY CHARGERFPLSubstantially Equivalent
K781562HEMACHECKGKLSubstantially Equivalent
K781332PEEP/CPAP VALVEBYESubstantially Equivalent
K781325MARKII VENTIMASKSBYFSubstantially Equivalent

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.

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Data as of , FDA export datePage updated Source: openFDA, public domain