Simmler & Son, Inc.
Simmler & Son, Inc. holds FDA 510(k) medical device clearances, first cleared 1976, most recent 1978.
Top product codes for Simmler & Son, Inc.
Recent clearances by Simmler & Son, Inc.
- K780817 — GLOBIN-TERGE
- K771903 — LIPASE
- K771904 — GLYCEROL KINASE
- K771905 — GLYCEROL SUBSTRATE
- K771906 — PHOSPHATE
- K761086 — REAGENTS
- K760476 — REAGENT, LACTATE DEHYDROGENASE
- K760473 — REAGENT, ALBUMIN DETERMINATION
- K760474 — REAGENT, ALKALINE PHOSPHATASE DETERM.
- K760475 — REAGENT, CALCIUM DETERMINATION
- K760477 — REAGENTS-4 FOR URIC ACID DETERMINATION
- K760478 — REAGENT, BUN (UREA NITROGEN) DETERM.
- K760479 — REAGENT, TOTAL BILIRUBIN DETERMINATION
- K760480 — REAGENT, TOTAL PROTEIN DETERMINATION
Data sourced from openFDA. This site is unofficial and independent of the FDA.