ASAHI PTCA Guide Wire ASAHI SUOH 03
K-Number: K162842 · 2017-01-27
ApplicantAsahi Intecc Co., Ltd.
Decision Date2017-01-27
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
ASAHI PTCA Guide Wire ASAHI SUOH 03 is a medical device manufactured by Asahi Intecc Co., Ltd.. It received FDA 510(k) clearance on 2017-01-27 under approval number K162842. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the ASAHI PTCA Guide Wire ASAHI SUOH 03?
ASAHI PTCA Guide Wire ASAHI SUOH 03 is a medical device that received FDA 510(k) clearance on 2017-01-27. It is manufactured by Asahi Intecc Co., Ltd.. The 510(k) number is K162842.
When was ASAHI PTCA Guide Wire ASAHI SUOH 03 approved by the FDA?
ASAHI PTCA Guide Wire ASAHI SUOH 03 received FDA 510(k) clearance on 2017-01-27, under approval number K162842.
What company makes ASAHI PTCA Guide Wire ASAHI SUOH 03?
ASAHI PTCA Guide Wire ASAHI SUOH 03 is manufactured by Asahi Intecc Co., Ltd..
What is the FDA product code for ASAHI PTCA Guide Wire ASAHI SUOH 03?
The FDA product code for ASAHI PTCA Guide Wire ASAHI SUOH 03 is DQX.
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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.