HS30 Diagnostic Ultrasound System
K-Number: K202556 · 2020-10-30
ApplicantSamsung Medison Co., Ltd.
Decision Date2020-10-30
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
HS30 Diagnostic Ultrasound System is a medical device manufactured by Samsung Medison Co., Ltd.. It received FDA 510(k) clearance on 2020-10-30 under approval number K202556. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the HS30 Diagnostic Ultrasound System?
HS30 Diagnostic Ultrasound System is a medical device that received FDA 510(k) clearance on 2020-10-30. It is manufactured by Samsung Medison Co., Ltd.. The 510(k) number is K202556.
When was HS30 Diagnostic Ultrasound System approved by the FDA?
HS30 Diagnostic Ultrasound System received FDA 510(k) clearance on 2020-10-30, under approval number K202556.
What company makes HS30 Diagnostic Ultrasound System?
HS30 Diagnostic Ultrasound System is manufactured by Samsung Medison Co., Ltd..
What is the FDA product code for HS30 Diagnostic Ultrasound System?
The FDA product code for HS30 Diagnostic Ultrasound System is IYN.
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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.