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Medasonics, Inc.

Mchenry, IL, US

Medasonics, Inc. appears in FDA device records in Mchenry, IL. FDA records list 19 510(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
19
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 19 510(k) clearances for Medasonics, Inc. between 1978 and 1999. The busiest year on record is 1980, with 3. The most recent is 1999, with 1.

Clearances by year, as a table
510(k) clearance decisions for Medasonics, Inc., by decision year
YearClearances
19781
19791
19803
19812
19821
19833
19861
19871
19881
19911
19921
19961
19971
19991
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K991441CADENCE DOPPLER ULTRASOUND SYSTEMKNGSubstantially Equivalent
K962796NEUROGUARD TRANSCRANIAL DOPPLER ULTRASOUND SYSTEMIYNSubstantially Equivalent
K961116FIRST BEAT/CARDIO BEAT/CALCIYOSubstantially Equivalent
K914862CEREBROVASCULAR DIAGNOSTIC SYSTEM; CDSIYNSubstantially Equivalent
K911453OBTRASOUND STETHOSCOPE FETAL CALCKNGSubstantially Equivalent
K882018MEDACORD PVL, PERSONAL VASCULAR LABORATORYJAFSubstantially Equivalent
K872292TRANSPECT TRANSCRANIAL DOPPLERIYNSubstantially Equivalent
K854734MODEL 5320 TED SEQUENTIAL COMP. DE. COMP. LIMB SLEDRMSubstantially Equivalent
K833588VASCULAR LABORATORY TREADMILL VT1IOLSubstantially Equivalent
K837481BF24 DOPPLER MODEL P872 AND P874Substantially Equivalent
K831393VASCULAB BLOOD PRESSURE CUFFDXQSubstantially Equivalent
K820898VASCULAB SPECTRUM ANALYZER #SP25DXGSubstantially Equivalent
K812609VASCULAB #VSC21JOMSubstantially Equivalent
K812608VASCULAB #R12BDSFSubstantially Equivalent
K801549MODEL R11 SINGLE CHANNEL CHART RECORDERDSFSubstantially Equivalent
K800768VASCULAB BI-DIRECTIONAL DOPPLER, #D10JAFSubstantially Equivalent
K800767MOD. MCI 17 MANUAL CUFF INFLATORDXQSubstantially Equivalent
K782132PLETHYSMOGRAPH, STRAIN GAUGEJOMSubstantially Equivalent
K781358SEQUENTIAL CUFF INFLATION DEVICEJOWSubstantially 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

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