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Innovative Medical Systems, Inc.

Mchenry, IL, US

Innovative Medical Systems, Inc. appears in FDA device records in Mchenry, IL. FDA records list 22 510(k) clearances between and , 6 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
6
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 22 510(k) clearances for Innovative Medical Systems, Inc. between 1978 and 1997. The busiest year on record is 1992, with 5. The most recent is 1997, with 1.

Clearances by year, as a table
510(k) clearance decisions for Innovative Medical Systems, Inc., by decision year
YearClearances
19783
19801
19823
19831
19841
19853
19882
19925
19941
19951
19971
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K973035VIOLA II DENTAL CAMERA SYSTEMEIASubstantially Equivalent
K951469BAZOOKA SYSTEMFNMSubstantially Equivalent
K933184POSITIVE AIRWAY PRESSURE SYSTEMBZDSubstantially Equivalent
K924590MICROWAVE AUTOMATED TISSUE PROCESSORIEOSubstantially Equivalent
K922081LABOTECH AUTOMATED MICROTITER ANALYZERJJQSubstantially Equivalent
K921005AUTOLOADERJQWSubstantially Equivalent
K915457PHACO 20/20 SYSTEM IHQCSubstantially Equivalent
K915456PHACO 3000 LINEARHQCSubstantially Equivalent
K883599LX-80 AUTOMATED TISSUE PROCESSOR (PLASTIC)IEOSubstantially Equivalent
K880745LX-100 SLIDE STAINERKPASubstantially Equivalent
K853938LX 300 TISSUE PROCESSORIEOSubstantially Equivalent
K853463LX EMBEDDING CENTERSubstantially Equivalent
K851054LX120 TISSUE PROCESSORIEOSubstantially Equivalent
K842077MIDAS II AUTOMATIC STAINERKPASubstantially Equivalent
K832994MIDAS 6000 AUTOMATIC STAINERKPASubstantially Equivalent
K823522DILULAB 230GKHSubstantially Equivalent
K823124IMS HEMATOLOGY MIXERGLESubstantially Equivalent
K821830MI DAS 1000 AUTOMATIC SLIDE STAINERKPASubstantially Equivalent
K801513TISSUE PROCESSING SYSTEMIEOSubstantially Equivalent
K781361HEMOGLOBINOMETER MODEL 720 BGKRSubstantially Equivalent
K780882DILUTER/DISPENSERJQWSubstantially Equivalent
K780789PERALISTIC PUMP MODEL 2000JQWSubstantially 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