The following data is part of a premarket notification filed by Electric Mobility Corp. with the FDA for Electric Mobility's Sparky.
| Device ID | K874739 |
| 510k Number | K874739 |
| Device Name: | ELECTRIC MOBILITY'S SPARKY |
| Classification | Wheelchair, Powered |
| Applicant | ELECTRIC MOBILITY CORP. #1 MOBILITY PLAZA Sewell, NJ 08080 |
| Contact | Michael Flowers |
| Correspondent | Michael Flowers ELECTRIC MOBILITY CORP. #1 MOBILITY PLAZA Sewell, NJ 08080 |
| Product Code | ITI |
| CFR Regulation Number | 890.3860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-11-18 |
| Decision Date | 1988-04-22 |