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 the device name listed in this FDA 510(k) record. The listed applicant is Intelligent Ultrasound Limited. It received FDA 510(k) clearance on 2023-10-06 under 510(k) 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. The listed applicant is Intelligent Ultrasound Limited. The 510(k) number is K232787.

When did ScanNav Anatomy Peripheral Nerve Block receive FDA 510(k) clearance?

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

Who is the listed applicant for ScanNav Anatomy Peripheral Nerve Block?

The FDA 510(k) record lists Intelligent Ultrasound Limited as the applicant. This does not by itself establish the device manufacturer.

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 Devices (Code: QRG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K250818NervebloxSmart Alfa Teknoloji San. Ve Tic. A.S.

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.