FDA 510(k)

DERMATRON IONTOPHORESIS DEVICE

K-Number: K780310 · 1978-07-31

Decision Date1978-07-31

Product Code

DecisionSubstantially Equivalent

Device Summary

DERMATRON IONTOPHORESIS DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Motion Control, Inc.. It received FDA 510(k) clearance on 1978-07-31 under 510(k) number K780310. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DERMATRON IONTOPHORESIS DEVICE?

DERMATRON IONTOPHORESIS DEVICE is a medical device that received FDA 510(k) clearance on 1978-07-31. The listed applicant is Motion Control, Inc.. The 510(k) number is K780310.

When did DERMATRON IONTOPHORESIS DEVICE receive FDA 510(k) clearance?

DERMATRON IONTOPHORESIS DEVICE received FDA 510(k) clearance on 1978-07-31, under 510(k) number K780310.

Who is the listed applicant for DERMATRON IONTOPHORESIS DEVICE?

The FDA 510(k) record lists Motion Control, Inc. as the applicant. This does not by itself establish the device manufacturer.

Related Clinical Trials

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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Other records listing Motion Control, Inc. as applicant

K872040PHORESOR II (TM), MODEL PM700 K862236MYOLAB II, MODEL ML-200 K802642UTAH ARTIFICAL ARM

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.