S90 Exp Series Digital Color Doppler Ultrasound System
K-Number: K222596 · 2023-02-10
Device Summary
Frequently Asked Questions
What is the S90 Exp Series Digital Color Doppler Ultrasound System?
S90 Exp Series Digital Color Doppler Ultrasound System is a medical device that received FDA 510(k) clearance on 2023-02-10. The listed applicant is Sonoscape Medical Corp.. The 510(k) number is K222596.
When did S90 Exp Series Digital Color Doppler Ultrasound System receive FDA 510(k) clearance?
S90 Exp Series Digital Color Doppler Ultrasound System received FDA 510(k) clearance on 2023-02-10, under 510(k) number K222596.
Who is the listed applicant for S90 Exp Series Digital Color Doppler Ultrasound System?
The FDA 510(k) record lists Sonoscape Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for S90 Exp Series Digital Color Doppler Ultrasound System?
The FDA product code for S90 Exp Series Digital Color Doppler Ultrasound System is IYN.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Sonoscape Medical Corp. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: IYN)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.