The following data is part of a premarket notification filed by Sunrise Medical Quickie Designs, Inc. with the FDA for Zippie P500.
| Device ID | K920179 |
| 510k Number | K920179 |
| Device Name: | ZIPPIE P500 |
| Classification | Wheelchair, Mechanical |
| Applicant | SUNRISE MEDICAL QUICKIE DESIGNS, INC. 2842 BUSINESS PARK AVE. Fresno, CA 93727 |
| Contact | Pat Spink |
| Correspondent | Pat Spink SUNRISE MEDICAL QUICKIE DESIGNS, INC. 2842 BUSINESS PARK AVE. Fresno, CA 93727 |
| Product Code | IOR |
| CFR Regulation Number | 890.3850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-01-14 |
| Decision Date | 1992-04-29 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ZIPPIE P500 74244182 1761236 Dead/Cancelled |
SUNRISE MEDICAL HHG INC. 1992-02-07 |