AVIEW RT ACS
K-Number: K220408 · 2022-11-10
ApplicantCoreline Soft Co., Ltd.
Decision Date2022-11-10
Product CodeQKB
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
AVIEW RT ACS is a medical device manufactured by Coreline Soft Co., Ltd.. It received FDA 510(k) clearance on 2022-11-10 under approval number K220408. The device is classified under product code QKB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the AVIEW RT ACS?
AVIEW RT ACS is a medical device that received FDA 510(k) clearance on 2022-11-10. It is manufactured by Coreline Soft Co., Ltd.. The 510(k) number is K220408.
When was AVIEW RT ACS approved by the FDA?
AVIEW RT ACS received FDA 510(k) clearance on 2022-11-10, under approval number K220408.
What company makes AVIEW RT ACS?
AVIEW RT ACS is manufactured by Coreline Soft Co., Ltd..
What is the FDA product code for AVIEW RT ACS?
The FDA product code for AVIEW RT ACS is QKB.
Other Devices by Coreline Soft Co., Ltd.
Related Devices (Code: QKB)
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.