The following data is part of a premarket notification filed by Etac Us, Inc. with the FDA for Swede Cross Manual Wheelchair.
Device ID | K914610 |
510k Number | K914610 |
Device Name: | SWEDE CROSS MANUAL WHEELCHAIR |
Classification | Wheelchair, Mechanical |
Applicant | ETAC US, INC. 2325 PARKLAWN DRIVE, SUITE P Waukesha, WI 53186 |
Contact | Melody B Dill |
Correspondent | Melody B Dill ETAC US, INC. 2325 PARKLAWN DRIVE, SUITE P Waukesha, WI 53186 |
Product Code | IOR |
CFR Regulation Number | 890.3850 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-10-17 |
Decision Date | 1991-11-29 |