The following data is part of a premarket notification filed by Adaptive Switch Laboratories, Inc. with the FDA for Asl Model #102.
| Device ID | K914739 |
| 510k Number | K914739 |
| Device Name: | ASL MODEL #102 |
| Classification | Wheelchair, Powered |
| Applicant | ADAPTIVE SWITCH LABORATORIES, INC. 1181 BRITTMORE, STE. 500 Houston, TX 77043 |
| Contact | James A Swift |
| Correspondent | James A Swift ADAPTIVE SWITCH LABORATORIES, INC. 1181 BRITTMORE, STE. 500 Houston, TX 77043 |
| Product Code | ITI |
| CFR Regulation Number | 890.3860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-10-21 |
| Decision Date | 1991-12-16 |