DeltaFil, DeltaFil Conditioner
K-Number: K213201 · 2022-06-01
Decision Date2022-06-01
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
DeltaFil, DeltaFil Conditioner is a medical device manufactured by DMG Chemisch-Pharmazeutische Fabrik GmbH. It received FDA 510(k) clearance on 2022-06-01 under approval number K213201. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the DeltaFil, DeltaFil Conditioner?
DeltaFil, DeltaFil Conditioner is a medical device that received FDA 510(k) clearance on 2022-06-01. It is manufactured by DMG Chemisch-Pharmazeutische Fabrik GmbH. The 510(k) number is K213201.
When was DeltaFil, DeltaFil Conditioner approved by the FDA?
DeltaFil, DeltaFil Conditioner received FDA 510(k) clearance on 2022-06-01, under approval number K213201.
What company makes DeltaFil, DeltaFil Conditioner?
DeltaFil, DeltaFil Conditioner is manufactured by DMG Chemisch-Pharmazeutische Fabrik GmbH.
What is the FDA product code for DeltaFil, DeltaFil Conditioner?
The FDA product code for DeltaFil, DeltaFil Conditioner is EMA.
Other Devices by DMG Chemisch-Pharmazeutische Fabrik GmbH
Related Devices (Code: EMA)
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.