Company ยท US
Motion Control, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1978 to 1987. Name variants (Inc, Corp, punctuation) are merged.
4510(k) clearances (0 in 12 months)
1recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 4, 1987 | K872040 | PHORESOR II (TM), MODEL PM700 Motion Control, Inc. | EGJ |
| Aug 7, 1986 | K862236 | MYOLAB II, MODEL ML-200 Motion Control, Inc. | IKN |
| Nov 12, 1980 | K802642 | UTAH ARTIFICAL ARM Motion Control, Inc. | IRE |
| Jul 31, 1978 | K780310 | DERMATRON IONTOPHORESIS DEVICE Motion Control, Inc. |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 6, 2005 | Motion Control, Inc. Spectre brand AC wall adapter to be used with ProControl 2 or ProHand battery powered upper limb prosthesis. Terminated |
IQZ | None listed |