The following data is part of a premarket notification filed by Technicare Corp. with the FDA for Needle Guide Attachment.
| Device ID | K811931 |
| 510k Number | K811931 |
| Device Name: | NEEDLE GUIDE ATTACHMENT |
| 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 | 1981-07-06 |
| Decision Date | 1981-08-18 |