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FDA 510(k)

BTL-899A

K-Number: K213344 · 2022-01-05

ApplicantBTL Industries, Inc.
Decision Date2022-01-05
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BTL-899A is a medical device manufactured by BTL Industries, Inc.. It received FDA 510(k) clearance on 2022-01-05 under approval number K213344. 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-899A?

BTL-899A is a medical device that received FDA 510(k) clearance on 2022-01-05. It is manufactured by BTL Industries, Inc.. The 510(k) number is K213344.

When was BTL-899A approved by the FDA?

BTL-899A received FDA 510(k) clearance on 2022-01-05, under approval number K213344.

What company makes BTL-899A?

BTL-899A is manufactured by BTL Industries, Inc..

What is the FDA product code for BTL-899A?

The FDA product code for BTL-899A 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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