The following data is part of a premarket notification filed by Fortress Scientific Ltd. with the FDA for 730 Power Base.
| Device ID | K933858 |
| 510k Number | K933858 |
| Device Name: | 730 POWER BASE |
| Classification | Wheelchair, Powered |
| Applicant | FORTRESS SCIENTIFIC LTD. C/O FOLEY & LARDNER 3000 K STREET, N.W. Washington, DC 20007 |
| Contact | Ilene Knable Gotts |
| Correspondent | Ilene Knable Gotts FORTRESS SCIENTIFIC LTD. C/O FOLEY & LARDNER 3000 K STREET, N.W. Washington, DC 20007 |
| Product Code | ITI |
| CFR Regulation Number | 890.3860 [🔎] |
| Decision | Substantially Equivalent For Some Indications (SN) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-08-06 |
| Decision Date | 1994-03-28 |