Medical Device
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Imed Corp.

Mchenry, IL, US

Imed Corp. appears in FDA device records in Mchenry, IL. FDA records list 15 510(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
15
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 15 510(k) clearances for Imed Corp. between 1977 and 1983. The busiest year on record is 1982, with 4. The most recent is 1983, with 2.

Clearances by year, as a table
510(k) clearance decisions for Imed Corp., by decision year
YearClearances
19772
19782
19792
19801
19812
19824
19832
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K831935ENTERNAL PUMP & ADMIN. SET 430FRNSubstantially Equivalent
K831596DROP RATE COUNTER #340FLNSubstantially Equivalent
K823346ACCUSET ADMINISTRATION SETFPASubstantially Equivalent
K823347MACRODOT ADD-I-MED ADMIN. SETFPASubstantially Equivalent
K823026380 PIGGYBACK CONTROLLERLDRSubstantially Equivalent
K813445IV FILTERSET 5 MICROMETERFPBSubstantially Equivalent
K812824PRESSURE DISC COMPONENT FOR ACCUSETFRNSubstantially Equivalent
K812823IMED MODEL 970 & 975 VOL. INFUSION PUMPFRNSubstantially Equivalent
K801734IMED DROP RATE CALCULATOR #340FLNSubstantially Equivalent
K790669DROP CONTROLLERFLNSubstantially Equivalent
K790108FILTERSET 0.22, I.V. PUMPFPASubstantially Equivalent
K781589VOLUMETRIC CONTROLLER MODEL 310FLNSubstantially Equivalent
K781171INFUSION PUMP, PEDIATRIC MODEL 301FRNSubstantially Equivalent
K771664VOLUMETRIC INFUSION PUMP MODEL 960FRNSubstantially Equivalent
K771453FLUID HANDLING DEVICE W/INPUT TUBINGFPASubstantially 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