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 |