SC930 Seat Controller
by Fortress Scientific, Ltd. 510(k)
Active
510(k) K933859
Overview
The SC930 Seat Controller is a powered wheelchair device classified under product code ITI and medical specialty Physical Medicine. It received FDA 510(k) clearance as substantially equivalent for some indications on March 28, 1994, under K933859.
The device is manufactured by Fortress Scientific, Ltd., and is authorized for distribution in the United States. It is a class II medical device with regulation number 890.3860 and was cleared via the traditional 510(k) pathway.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SN | NumberK933859 | Date28 Mar 1994 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — FDA 510(k) Active
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- 510(k) Number
- FDA Product Code
- ITI
- FDA applicant
- Fortress Scientific , Ltd.
- Device Class
- Class II
- Regulation
- 21 CFR Part 890.3860
- Advisory Committee
- Physical Medicine
- FDA Decision
- SN
Other devices from Fortress Scientific, Ltd.
Questions
What is the SC930 Seat Controller used for?
The SC930 Seat Controller is a powered wheelchair device designed to control seat positioning functions in powered wheelchairs, as indicated by its classification under product code ITI and medical specialty Physical Medicine.
How was the SC930 Seat Controller authorized for use in the United States?
The SC930 Seat Controller received FDA 510(k) clearance on March 28, 1994, under submission K933859, being found substantially equivalent for some indications via the traditional 510(k) pathway.
What regulatory classification does the SC930 Seat Controller have?
The SC930 Seat Controller is classified as a class II medical device with regulation number 890.3860 and product code ITI, as specified in its FDA authorization details.