The following data is part of a premarket notification filed by Technicare Corp. with the FDA for Technicare 248 Sl & 260sl.
| Device ID | K841817 |
| 510k Number | K841817 |
| Device Name: | TECHNICARE 248 SL & 260SL |
| Classification | System, Imaging, Pulsed Echo, Ultrasonic |
| Applicant | TECHNICARE CORP. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | IYO |
| CFR Regulation Number | 892.1560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-05-01 |
| Decision Date | 1984-08-17 |