The following data is part of a premarket notification filed by Teratech Corp. with the FDA for Prosound C3 / C3 Cv Ultrasound Systems.
| Device ID | K110482 |
| 510k Number | K110482 |
| Device Name: | PROSOUND C3 / C3 CV ULTRASOUND SYSTEMS |
| Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
| Applicant | TERATECH CORP. P.O. BOX 10074 13221 NE TEEM LOOP ROAD Bainbridge Island, WA 98110 |
| Contact | Charles F Hottinger |
| Correspondent | Mark Job REGULATORY TECHNOLOGY SERVICES, LLC 1000 Westgate Drive, Suite 510k Saint Paul, MN 55114 |
| Product Code | IYN |
| Subsequent Product Code | ITX |
| Subsequent Product Code | IYO |
| CFR Regulation Number | 892.1550 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2011-02-18 |
| Decision Date | 2011-03-18 |
| Summary: | summary |