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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 a medical device manufactured by Smart Alfa Teknoloji San. Ve Tic. A.S.. It received FDA 510(k) clearance on 2025-08-15 under approval 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. It is manufactured by Smart Alfa Teknoloji San. Ve Tic. A.S.. The 510(k) number is K250818.

When was Nerveblox approved by the FDA?

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

What company makes Nerveblox?

Nerveblox is manufactured by Smart Alfa Teknoloji San. Ve Tic. A.S..

What is the FDA product code for Nerveblox?

The FDA product code for Nerveblox is QRG.

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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.

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