510(k) Report

510(k) · Cleared

Cleared

Dermatron Iontophoresis Device

K780310510(k) TraditionalCleared Jul 31, 1978160-day review

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Motion Control, Inc.

Cleared on Jul 31, 1978 after a 160-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Jul 31, 1978
Review
160 days
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 1999: 1 descendant cleared19801990200020102020
  1. This deviceK780310 Dermatron Iontophoresis DeviceMotion Control, Inc. · 1978
  2. Descendant · cites it directly · 0 of its ownK991991 Dupel Iontophoresis SystemEmpi · 1999

Most influential descendants

Showing 1 of 1 · See all
  • K991991Dupel Iontophoresis SystemEmpi · 1999 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K780310Dermatron Iontophoresis DeviceMotion Control, Inc.1978—
+1K991991Dupel Iontophoresis SystemEmpi1999—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199910
FIG. 1 — Lineage of K780310, 1978–1999Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in this category? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
Get a 510(k) Report

What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K991991Dupel Iontophoresis SystemEmpi19990

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Of its descendants, K991991 (Empi, 1999) has gone furthest, with 0 descendants of its own.

More from Motion Control, Inc.

4 FDA decisions under this applicant name. See the company

  • K872040Phoresor II (TM), Model PM700Motion Control, Inc. · 1987
  • K862236Myolab II, Model ML-200Motion Control, Inc. · 1986
  • K802642Utah Artifical ArmMotion Control, Inc. · 1980

https://510kreport.com/device/K780310 · printed Nov 3, 2026

Cite this page

510(k) Report. “K780310: Dermatron Iontophoresis Device.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K780310

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026