Sonoscape Company Limited
Sonoscape Company Limited holds FDA 510(k) medical device clearances, first cleared 2004, most recent 2015.
Top product codes for Sonoscape Company Limited
Recent clearances by Sonoscape Company Limited
- K150045 — S30/S40 Digital Color Doppler Ultraound System
- K142714 — S8 Exp/S9 Pro Portable Digital Color Doppler Ultrasound System
- K142815 — S22 Digital Color Doppler Ultrasound System
- K142710 — S9 Portable Digital Color Doppler Ultrasound System
- K142474 — S12 Digital Color Doppler Ultrasound System
- K131262 — DIGITAL ELECTROCARDIOGRAPHS
- K132527 — DIGITAL COLOR DOPPLER ULTASOUND SYSTEM
- K132768 — S8 EXP PORTABLE DIGITAL COLOR DOPPLER ULTRASOUND SYSTEM
- K131213 — DIGITAL COLOR DOPPLER ULTRASOUND SYSTEM
- K130801 — DIGITAL COLOR DOPPLER ULTRASOUND SYSTEM
- K131088 — PORTABLE DIGITAL COLOR DOPPLER ULTRASOUND SYSTEM
- K130119 — PORTABLE DIGITAL COLOR DOPPLER ULTRASOUND SYSTEM
- K123616 — PORTABLE ULTRASONIC DIAGNOSTIC SYSTEM
- K112602 — S6 DIAGNOSTIC ULTRASOUND SYSTEM
- K112451 — S8 DIAGNOSTIC ULTRASOUND SYSTEM
- K110510 — S20 DIGITAL COLOR DOPPLER ULTRASOUND SYSTEM
- K102642 — SONOSCAPE ULTRASOUND SYSTEM AND TRANSDUCERS MODEL SSI-8000, 2P1 PHASED ARRAY, 5P1 PHASED ARRAY MODEL 2P1, 5P1, 6V1 MICRO
- K101337 — A6 PORTABLE ULTRASONIC DIAGNOSTIC SYSTEM
- K092922 — SSI-8000/S8/S6 DIGITAL COLOR DOPPLER ULTRASOUND SYSTEM, 2P1 PHASED ARRAY DIAGNOSTIC ULTRASOUND TRANSDUCER
- K052042 — SONOSCAPE SSI-1000/SSI-5000 ULTRASOUND TRANSDUCERS
- K042369 — SONOSCAPE ULTRASOUND SYSTEM SSI-1000/SSI-5000
- K041455 — SSI-600/SSI-800 DIAGNOSTIC ULTRASOUND IMAGING SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.