The following data is part of a premarket notification filed by Toronto Medical Corp. with the FDA for Mobilimb W1 Wrist Cpm Unit.
Device ID | K900466 |
510k Number | K900466 |
Device Name: | MOBILIMB W1 WRIST CPM UNIT |
Classification | Exerciser, 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 | BXB |
CFR Regulation Number | 890.5380 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-01-31 |
Decision Date | 1990-03-12 |