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FDA 510(k)

ScanNav Anatomy Peripheral Nerve Block

K-Number: K232787 · 2023-10-06

Decision Date2023-10-06
Product CodeQRG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ScanNav Anatomy Peripheral Nerve Block is a medical device manufactured by Intelligent Ultrasound Limited. It received FDA 510(k) clearance on 2023-10-06 under approval number K232787. The device is classified under product code QRG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ScanNav Anatomy Peripheral Nerve Block?

ScanNav Anatomy Peripheral Nerve Block is a medical device that received FDA 510(k) clearance on 2023-10-06. It is manufactured by Intelligent Ultrasound Limited. The 510(k) number is K232787.

When was ScanNav Anatomy Peripheral Nerve Block approved by the FDA?

ScanNav Anatomy Peripheral Nerve Block received FDA 510(k) clearance on 2023-10-06, under approval number K232787.

What company makes ScanNav Anatomy Peripheral Nerve Block?

ScanNav Anatomy Peripheral Nerve Block is manufactured by Intelligent Ultrasound Limited.

What is the FDA product code for ScanNav Anatomy Peripheral Nerve Block?

The FDA product code for ScanNav Anatomy Peripheral Nerve Block is QRG.

Related Clinical Trials

Related PubMed Literature

Other Devices by Intelligent Ultrasound Limited

Related Devices (Code: QRG)

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.