MAA — Monitor, Fetal Doppler Ultrasound Class II
FDA Device Classification
Classification Details
- Product Code
- MAA
- Device Class
- Class II
- Regulation Number
- 884.2660
- Submission Type
- Review Panel
- RA
- Medical Specialty
- Obstetrics/Gynecology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K102138 | edan instruments | ULTRASONIC TABLETOP DOPPLER; ULTRASONIC TABLETOP DOPPLER | October 28, 2010 |
| K090499 | summit doppler systems | LIFEDOP MODEL, L350R | March 31, 2009 |
| K915138 | ge medical systems | GE SONOCHROME | October 20, 1992 |
| K905536 | toshiba america medical systems, in.c | FETAL DOPPLER | April 21, 1992 |
| K904600 | acuson | L582 TRANSDUCER | June 24, 1991 |
| K905456 | acuson | L328 TRANSDUCER | May 28, 1991 |
| K904951 | acuson | S5192R TRANSDUCER | April 29, 1991 |
| K895909 | oxford medilog | SONICAID MODEL VASOFLO 4 | July 9, 1990 |
| K894992 | quantum medical systems | QUANTUM QAD ANGIODYNOGRAPH ULTRASOUND SYSTEM | February 23, 1990 |