AirSeal iFS System; AirSeal dV Solution
K-Number: K230239 · 2023-09-20
ApplicantConmed Corporation
Decision Date2023-09-20
Product CodeHIF
Advisory CommitteeOB
DecisionSubstantially Equivalent
Device Summary
AirSeal iFS System; AirSeal dV Solution is a medical device manufactured by Conmed Corporation. It received FDA 510(k) clearance on 2023-09-20 under approval number K230239. The device is classified under product code HIF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the AirSeal iFS System; AirSeal dV Solution?
AirSeal iFS System; AirSeal dV Solution is a medical device that received FDA 510(k) clearance on 2023-09-20. It is manufactured by Conmed Corporation. The 510(k) number is K230239.
When was AirSeal iFS System; AirSeal dV Solution approved by the FDA?
AirSeal iFS System; AirSeal dV Solution received FDA 510(k) clearance on 2023-09-20, under approval number K230239.
What company makes AirSeal iFS System; AirSeal dV Solution?
AirSeal iFS System; AirSeal dV Solution is manufactured by Conmed Corporation.
What is the FDA product code for AirSeal iFS System; AirSeal dV Solution?
The FDA product code for AirSeal iFS System; AirSeal dV Solution is HIF.
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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.