The following data is part of a premarket notification filed by Davismade, Inc. with the FDA for Power Standing Dani.
Device ID | K090256 |
510k Number | K090256 |
Device Name: | POWER STANDING DANI |
Classification | Wheelchair, Standup |
Applicant | DAVISMADE, INC. 2511 DAVISON RD Flint, MI 48506 |
Contact | Daniel Davis |
Correspondent | Daniel Davis DAVISMADE, INC. 2511 DAVISON RD Flint, MI 48506 |
Product Code | IPL |
CFR Regulation Number | 890.3900 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2009-02-02 |
Decision Date | 2009-07-06 |
Summary: | summary |