FDA 510(k)

D²RS and D²RS 9090

K-Number: K221335 · 2022-06-07

Decision Date2022-06-07

Product CodeOWB

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

D²RS and D²RS 9090 is a medical device manufactured by Stephanix. It received FDA 510(k) clearance on 2022-06-07 under approval number K221335. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the D²RS and D²RS 9090?

D²RS and D²RS 9090 is a medical device that received FDA 510(k) clearance on 2022-06-07. It is manufactured by Stephanix. The 510(k) number is K221335.

When was D²RS and D²RS 9090 approved by the FDA?

D²RS and D²RS 9090 received FDA 510(k) clearance on 2022-06-07, under approval number K221335.

What company makes D²RS and D²RS 9090?

D²RS and D²RS 9090 is manufactured by Stephanix.

What is the FDA product code for D²RS and D²RS 9090?

The FDA product code for D²RS and D²RS 9090 is OWB.

Other Devices by Stephanix

K213479D²RS and D²RS 9090 K212515MOVIX DReamy

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.