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510(k) K780310

DERMATRON IONTOPHORESIS DEVICE by Motion Control, Inc.

K780310 is an FDA 510(k) premarket notification submitted by Motion Control, Inc. for the device "DERMATRON IONTOPHORESIS DEVICE". The FDA issued a decision of Substantially Equivalent on July 31, 1978. Motion Control, Inc. has at least 3 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 31, 1978
Date Received
February 21, 1978
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Motion Control, Inc.

  • K872040 — PHORESOR II (TM), MODEL PM700 (August 4, 1987)
  • K862236 — MYOLAB II, MODEL ML-200 (August 7, 1986)
  • K802642 — UTAH ARTIFICAL ARM (November 12, 1980)

FDA data resources