The following data is part of a premarket notification filed by Medi-man Rehabilitation Products, Inc. with the FDA for Medi-plinth.
| Device ID | K924905 |
| 510k Number | K924905 |
| Device Name: | MEDI-PLINTH |
| Classification | Table, Powered |
| Applicant | MEDI-MAN REHABILITATION PRODUCTS, INC. 5630 TOMKEN ROAD MISSISSAUGA, ONTARIO, Canada, L4w 1p4, CA |
| Contact | Jane Belrose |
| Correspondent | Jane Belrose MEDI-MAN REHABILITATION PRODUCTS, INC. 5630 TOMKEN ROAD MISSISSAUGA, ONTARIO, Canada, L4w 1p4, CA |
| Product Code | INQ |
| CFR Regulation Number | 890.3760 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-09-29 |
| Decision Date | 1993-02-16 |