The following data is part of a premarket notification filed by Toronto Medical Corp. with the FDA for Mobilimb H3 Hand Cpm Unit.
| Device ID | K900794 |
| 510k Number | K900794 |
| Device Name: | MOBILIMB H3 HAND CPM UNIT |
| Classification | Exerciser, Finger, Powered |
| Applicant | TORONTO MEDICAL CORP. 901 DILLINGHAM ROAD PICKERING, ONTARIO Canada L1w 2y5, CA |
| Contact | Jeff Harmon |
| Correspondent | Jeff Harmon TORONTO MEDICAL CORP. 901 DILLINGHAM ROAD PICKERING, ONTARIO Canada L1w 2y5, CA |
| Product Code | JFA |
| CFR Regulation Number | 890.5410 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-02-20 |
| Decision Date | 1990-03-02 |