510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K780310Substantially Equivalent

Dermatron Iontophoresis Device

Motion Control, Inc., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K780310 is the FDA 510(k) clearance record for DERMATRON IONTOPHORESIS DEVICE, cleared for Motion Control, Inc. on . FDA records list 4 510(k) clearances for Motion Control, Inc., from to . As of , FDA records show no recalls naming K780310.

Clearance record

Decision date
Received
(160 days to decision)
Review panel
Unknown
Applicant
Motion Control, Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No