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FDA 510(k)

MEDION MI-200 IONTOPHORETIC MEDICATOR

K-Number: K831000 · 1983-08-08

ApplicantEtherington Industries
Decision Date1983-08-08
Product Code
DecisionSubstantially Equivalent

Device Summary

MEDION MI-200 IONTOPHORETIC MEDICATOR is the device name listed in this FDA 510(k) record. The listed applicant is Etherington Industries. It received FDA 510(k) clearance on 1983-08-08 under 510(k) number K831000. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDION MI-200 IONTOPHORETIC MEDICATOR?

MEDION MI-200 IONTOPHORETIC MEDICATOR is a medical device that received FDA 510(k) clearance on 1983-08-08. The listed applicant is Etherington Industries. The 510(k) number is K831000.

When did MEDION MI-200 IONTOPHORETIC MEDICATOR receive FDA 510(k) clearance?

MEDION MI-200 IONTOPHORETIC MEDICATOR received FDA 510(k) clearance on 1983-08-08, under 510(k) number K831000.

Who is the listed applicant for MEDION MI-200 IONTOPHORETIC MEDICATOR?

The FDA 510(k) record lists Etherington Industries as the applicant. This does not by itself establish the device manufacturer.

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Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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