Medical Device Manufacturer · US , Mchenry , IL

Simmler & Son, Inc. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1976

Total

Cleared

Denied

Simmler & Son, Inc. has 14 FDA 510(k) cleared chemistry devices. Based in Mchenry, US.

Historical record: 14 cleared submissions from 1976 to 1978.

Browse the complete list of FDA 510(k) cleared chemistry devices from this manufacturer. Filter by specialty or product code using the sidebar.

Simmler & Son, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Simmler & Son, Inc.

14 devices

1-14 of 14

REAGENT, LACTATE DEHYDROGENASE

K760476 · CFJ

Chemistry · 76d

Cleared Oct 29, 1976

REAGENT, ALBUMIN DETERMINATION

K760473 · CIX

Chemistry · 73d

Cleared Oct 29, 1976

REAGENT, ALKALINE PHOSPHATASE DETERM.

K760474 · CJE

Chemistry · 73d

Cleared Oct 29, 1976

REAGENT, CALCIUM DETERMINATION

K760475 · CIC

Chemistry · 73d

Cleared Oct 29, 1976

REAGENTS-4 FOR URIC ACID DETERMINATION

K760477 · CDH

Chemistry · 73d

Cleared Oct 29, 1976

REAGENT, BUN (UREA NITROGEN) DETERM.

K760478 · CDW

Chemistry · 73d

Cleared Oct 29, 1976

REAGENT, TOTAL BILIRUBIN DETERMINATION

K760479 · CIG

Chemistry · 73d

Cleared Oct 29, 1976

REAGENT, TOTAL PROTEIN DETERMINATION

K760480 · CEK

Chemistry · 73d

Simmler & Son, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Simmler & Son, Inc.

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