The following data is part of a premarket notification filed by Compumedics Germany Gmgh with the FDA for Doppler-box.
| Device ID | K051085 |
| 510k Number | K051085 |
| Device Name: | DOPPLER-BOX |
| Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
| Applicant | COMPUMEDICS GERMANY GMGH JOSEF-SCHUETTLER STR. 2 Singen, DE 78224 |
| Contact | Gerold Widenhorn |
| Correspondent | Stefan Preiss TUV AMERICA, INC. 1775 OLD HIGHWAY 8 New Brighton, MN 55112 -1891 |
| Product Code | IYN |
| CFR Regulation Number | 892.1550 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2005-04-28 |
| Decision Date | 2005-05-05 |
| Summary: | summary |