FDA 510(k)

Ziehm Vision RFD 3D

K-Number: K231701 · 2023-07-10

Decision Date2023-07-10

Product CodeOWB

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

Ziehm Vision RFD 3D is a medical device manufactured by Ziehm Imaging GmbH. It received FDA 510(k) clearance on 2023-07-10 under approval number K231701. 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 Ziehm Vision RFD 3D?

Ziehm Vision RFD 3D is a medical device that received FDA 510(k) clearance on 2023-07-10. It is manufactured by Ziehm Imaging GmbH. The 510(k) number is K231701.

When was Ziehm Vision RFD 3D approved by the FDA?

Ziehm Vision RFD 3D received FDA 510(k) clearance on 2023-07-10, under approval number K231701.

What company makes Ziehm Vision RFD 3D?

Ziehm Vision RFD 3D is manufactured by Ziehm Imaging GmbH.

What is the FDA product code for Ziehm Vision RFD 3D?

The FDA product code for Ziehm Vision RFD 3D is OWB.

Other Devices by Ziehm Imaging GmbH

K161976Ziehm Solo FD K193230Ziehm Vision FD K190497Ziehm 8000 K202360Ziehm Vision RFD 3D K203428Ziehm Vision RFD K231700Ziehm Vision FD

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Related Devices (Code: OWB)

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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.