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 |