The following data is part of a premarket notification filed by Invacare Corp. with the FDA for Kuschall Design K3/k4 Series Of Manual Wheelchairs.
| Device ID | K982336 |
| 510k Number | K982336 |
| Device Name: | KUSCHALL DESIGN K3/K4 SERIES OF MANUAL WHEELCHAIRS |
| Classification | Wheelchair, Mechanical |
| Applicant | INVACARE CORP. ONE INVACARE WAY P.O. BOX 4028 Elyria, OH 44036 |
| Contact | Edward A Kroll |
| Correspondent | Edward A Kroll INVACARE CORP. ONE INVACARE WAY P.O. BOX 4028 Elyria, OH 44036 |
| Product Code | IOR |
| CFR Regulation Number | 890.3850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-07-06 |
| Decision Date | 1998-08-21 |
| Summary: | summary |