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 |