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FDA 510(k)

BTL-499

K-Number: K233849 · 2024-04-23

ApplicantBTL Industries, Inc.
Decision Date2024-04-23
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BTL-499 is a medical device manufactured by BTL Industries, Inc.. It received FDA 510(k) clearance on 2024-04-23 under approval number K233849. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BTL-499?

BTL-499 is a medical device that received FDA 510(k) clearance on 2024-04-23. It is manufactured by BTL Industries, Inc.. The 510(k) number is K233849.

When was BTL-499 approved by the FDA?

BTL-499 received FDA 510(k) clearance on 2024-04-23, under approval number K233849.

What company makes BTL-499?

BTL-499 is manufactured by BTL Industries, Inc..

What is the FDA product code for BTL-499?

The FDA product code for BTL-499 is GEI.

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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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