The following data is part of a premarket notification filed by Nova Technology Corp. with the FDA for Nova Transfer System, Model Xxx.
| Device ID | K874448 |
| 510k Number | K874448 |
| Device Name: | NOVA TRANSFER SYSTEM, MODEL XXX |
| Classification | Wheelchair, Powered |
| Applicant | NOVA TECHNOLOGY CORP. 89 CABOT COURT, UNIT L Hauppauge, NY 11788 |
| Contact | Paul Dimatteo |
| Correspondent | Paul Dimatteo NOVA TECHNOLOGY CORP. 89 CABOT COURT, UNIT L Hauppauge, NY 11788 |
| Product Code | ITI |
| CFR Regulation Number | 890.3860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-10-29 |
| Decision Date | 1987-12-17 |