The following data is part of a premarket notification filed by Pmt, Inc. with the FDA for Micromat W/various Models.
| Device ID | K831117 |
| 510k Number | K831117 |
| Device Name: | MICROMAT W/VARIOUS MODELS |
| Classification | Pad, Kelly |
| Applicant | PMT, Inc. Box 464 Hopkins, MN 55343 |
| Contact | Carroll E Reynolds |
| Correspondent | Carroll E Reynolds PMT, Inc. Box 464 Hopkins, MN 55343 |
| Product Code | FNW |
| CFR Regulation Number | 878.4370 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-04-05 |
| Decision Date | 1984-05-30 |