The following data is part of a premarket notification filed by Motion Control, Inc. with the FDA for Phoresor Ii (tm), Model Pm700.
| Device ID | K872040 |
| 510k Number | K872040 |
| Device Name: | PHORESOR II (TM), MODEL PM700 |
| Classification | Device, Iontophoresis, Other Uses |
| Applicant | MOTION CONTROL, INC. 1290 WEST 2320 SOUTH, SUITE A Salt Lake City, UT 84119 |
| Contact | Richard D Luntz |
| Correspondent | Richard D Luntz MOTION CONTROL, INC. 1290 WEST 2320 SOUTH, SUITE A Salt Lake City, UT 84119 |
| Product Code | EGJ |
| CFR Regulation Number | 890.5525 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-05-27 |
| Decision Date | 1987-08-04 |