Vial Adapter Ø20 mm
K-Number: K190149 · 2019-10-15
Decision Date2019-10-15
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Vial Adapter Ø20 mm is a medical device manufactured by Avenir Performance Europeenne Medical (Apem). It received FDA 510(k) clearance on 2019-10-15 under approval number K190149. The device is classified under product code LHI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Vial Adapter Ø20 mm?
Vial Adapter Ø20 mm is a medical device that received FDA 510(k) clearance on 2019-10-15. It is manufactured by Avenir Performance Europeenne Medical (Apem). The 510(k) number is K190149.
When was Vial Adapter Ø20 mm approved by the FDA?
Vial Adapter Ø20 mm received FDA 510(k) clearance on 2019-10-15, under approval number K190149.
What company makes Vial Adapter Ø20 mm?
Vial Adapter Ø20 mm is manufactured by Avenir Performance Europeenne Medical (Apem).
What is the FDA product code for Vial Adapter Ø20 mm?
The FDA product code for Vial Adapter Ø20 mm is LHI.
Other Devices by Avenir Performance Europeenne Medical (Apem)
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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.