510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K831000Substantially Equivalent

Medion Mi-200 Iontophoretic Medicator

Etherington Industries, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K831000 is the FDA 510(k) clearance record for MEDION MI-200 IONTOPHORETIC MEDICATOR, cleared for Etherington Industries on . FDA records list one 510(k) clearance for Etherington Industries. As of , FDA records show no recalls naming K831000.

Clearance record

Decision date
Received
(132 days to decision)
Review panel
Unknown
Applicant
Etherington Industries 803 N. Front St. Suite 3, Mchenry IL
Third party review
No