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Siemens Medical Laboratories, Inc.

Mchenry, IL, US

Siemens Medical Laboratories, Inc. appears in FDA device records in Mchenry, IL. FDA records list 13 510(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
13
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 13 510(k) clearances for Siemens Medical Laboratories, Inc. between 1979 and 1991. The busiest year on record is 1979, with 4. The most recent is 1991, with 1.

Clearances by year, as a table
510(k) clearance decisions for Siemens Medical Laboratories, Inc., by decision year
YearClearances
19794
19811
19851
19862
19882
19891
19901
19911
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K910971Z XT RADIATION THERAPY TREATMENT TABLEJAISubstantially Equivalent
K903139BEAMVIEW & BEAMVIEW PLUS (AKA PROJECT 743)IYESubstantially Equivalent
K894230PATIENT DATA MANAGEMENT SYSTEM (PROJECT 735)IYESubstantially Equivalent
K882729MEVATRON, M 2 CLASSIYESubstantially Equivalent
K875272SONOLINE CFDXKSubstantially Equivalent
K862339MEVATRON KD-2IYESubstantially Equivalent
K854609MEVAMATIC 3JADSubstantially Equivalent
K852907SIEMENS MEVATRON MELHNSubstantially Equivalent
K812032MEVATRON 67EIYESubstantially Equivalent
K791967MEVATRON 74X MEDICAL LINEAR ACCELERATORIYESubstantially Equivalent
K790747MEVATRON 74IYESubstantially Equivalent
K790688MEVATRON 67IYESubstantially Equivalent
K790388MEVATRON 60IYESubstantially 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