Motion Control, Inc.
Salt Lake City, UT, US
MOTION CONTROL, INC. appears in FDA device records in Salt Lake City, UT. FDA records list 4 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show one recall for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 4 510(k) clearances for Motion Control, Inc. between 1978 and 1987. The busiest year on record is 1978, with 1. The most recent is 1987, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1978 | 1 |
| 1980 | 1 |
| 1986 | 1 |
| 1987 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K872040 | PHORESOR II (TM), MODEL PM700 | EGJ | Substantially Equivalent | |
| K862236 | MYOLAB II, MODEL ML-200 | IKN | Substantially Equivalent | |
| K802642 | UTAH ARTIFICAL ARM | IRE | Substantially Equivalent | |
| K780310 | DERMATRON IONTOPHORESIS DEVICE | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 1723997 | 3001237006 | MOTION CONTROL, INC. | 115 N WRIGHT BROTHERS DR, SALT LAKE CITY, UT 84116 US | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
Recall records
| Recall | Product | Reason | Classification | Initiated | Status |
|---|---|---|---|---|---|
| Z-0959-05 | Spectre brand AC wall adapter to be used with ProControl 2 or ProHand battery powered upper limb prosthesis. | Incorrect AC wall adapter was distributed with prostheses. Incorrect use of adapters could damage the battery and cause a potential fire hazard. | Terminated |
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain