The following data is part of a premarket notification filed by Bruno Independent Living Aids, Inc. with the FDA for Carony.
Device ID | K002205 |
510k Number | K002205 |
Device Name: | CARONY |
Classification | Wheelchair, Mechanical |
Applicant | BRUNO INDEPENDENT LIVING AIDS, INC. 1780 EXECUTIVE DR. Oconomowoc, WI 53066 |
Contact | Richard Keller |
Correspondent | Richard Keller BRUNO INDEPENDENT LIVING AIDS, INC. 1780 EXECUTIVE DR. Oconomowoc, WI 53066 |
Product Code | IOR |
CFR Regulation Number | 890.3850 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-07-21 |
Decision Date | 2000-08-10 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CARONY 79129686 4527481 Live/Registered |
Autoadapt AB 2013-03-04 |
CARONY 78041269 not registered Dead/Abandoned |
Autoadapt-BEV AB 2001-01-02 |