The following data is part of a premarket notification filed by Pillar Technology, Inc. with the FDA for Zippy, Model I88wa.
| Device ID | K012846 |
| 510k Number | K012846 |
| Device Name: | ZIPPY, MODEL I88WA |
| Classification | Wheelchair, Powered |
| Applicant | PILLAR TECHNOLOGY, INC. 1101 ILLINOIS P.O. BOX 187 Neodesha, KS 66757 |
| Contact | Chris Tinsley |
| Correspondent | Chris Tinsley PILLAR TECHNOLOGY, INC. 1101 ILLINOIS P.O. BOX 187 Neodesha, KS 66757 |
| Product Code | ITI |
| CFR Regulation Number | 890.3860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-08-23 |
| Decision Date | 2001-11-20 |