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Simmler & Son, Inc.

Mchenry, IL, US

Simmler & Son, Inc. appears in FDA device records in Mchenry, IL. FDA records list 14 510(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
14
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 14 510(k) clearances for Simmler & Son, Inc. between 1976 and 1978. The busiest year on record is 1976, with 8. The most recent is 1978, with 1.

Clearances by year, as a table
510(k) clearance decisions for Simmler & Son, Inc., by decision year
YearClearances
19768
19775
19781
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K780817GLOBIN-TERGESubstantially Equivalent
K771906PHOSPHATECDTSubstantially Equivalent
K771905GLYCEROL SUBSTRATECDTSubstantially Equivalent
K771904GLYCEROL KINASECDTSubstantially Equivalent
K771903LIPASECDTSubstantially Equivalent
K761086REAGENTSJJCSubstantially Equivalent
K760476REAGENT, LACTATE DEHYDROGENASECFJSubstantially Equivalent
K760480REAGENT, TOTAL PROTEIN DETERMINATIONCEKSubstantially Equivalent
K760479REAGENT, TOTAL BILIRUBIN DETERMINATIONCIGSubstantially Equivalent
K760478REAGENT, BUN (UREA NITROGEN) DETERM.CDWSubstantially Equivalent
K760477REAGENTS-4 FOR URIC ACID DETERMINATIONCDHSubstantially Equivalent
K760475REAGENT, CALCIUM DETERMINATIONCICSubstantially Equivalent
K760474REAGENT, ALKALINE PHOSPHATASE DETERM.CJESubstantially Equivalent
K760473REAGENT, ALBUMIN DETERMINATIONCIXSubstantially 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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What MDM checks, and what it does not

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