FDA 510(k)

Nerveblox

K-Number: K250818 · 2025-08-15

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

Decision Date2025-08-15

Product CodeQRG

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

Nerveblox is the device name listed in this FDA 510(k) record. The listed applicant is Smart Alfa Teknoloji San. Ve Tic. A.S.. It received FDA 510(k) clearance on 2025-08-15 under 510(k) number K250818. 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 Nerveblox?

Nerveblox is a medical device that received FDA 510(k) clearance on 2025-08-15. The listed applicant is Smart Alfa Teknoloji San. Ve Tic. A.S.. The 510(k) number is K250818.

When did Nerveblox receive FDA 510(k) clearance?

Nerveblox received FDA 510(k) clearance on 2025-08-15, under 510(k) number K250818.

Who is the listed applicant for Nerveblox?

The FDA 510(k) record lists Smart Alfa Teknoloji San. Ve Tic. A.S. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Nerveblox?

The FDA product code for Nerveblox is QRG.

Other records listing Smart Alfa Teknoloji San. Ve Tic. A.S. as applicant

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.

K260234MSK Go

Related Devices (Code: QRG)

K232787ScanNav Anatomy Peripheral Nerve BlockIntelligent Ultrasound Limited

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.