The following data is part of a premarket notification filed by Permobil Of America with the FDA for Permobil Superior.
| Device ID | K870227 |
| 510k Number | K870227 |
| Device Name: | PERMOBIL SUPERIOR |
| Classification | Wheelchair, Powered |
| Applicant | PERMOBIL OF AMERICA BOX 20 1644 MASSACHUSETTS AVENUE Lexington, MA 02173 |
| Contact | Finkelstein, Md |
| Correspondent | Finkelstein, Md PERMOBIL OF AMERICA BOX 20 1644 MASSACHUSETTS AVENUE Lexington, MA 02173 |
| Product Code | ITI |
| CFR Regulation Number | 890.3860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-01-21 |
| Decision Date | 1987-02-10 |