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FDA 510(k)

BTL-785W

K-Number: K211639 · 2022-03-07

ApplicantBTL Industries, Inc.
Decision Date2022-03-07
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BTL-785W is a medical device manufactured by BTL Industries, Inc.. It received FDA 510(k) clearance on 2022-03-07 under approval number K211639. 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-785W?

BTL-785W is a medical device that received FDA 510(k) clearance on 2022-03-07. It is manufactured by BTL Industries, Inc.. The 510(k) number is K211639.

When was BTL-785W approved by the FDA?

BTL-785W received FDA 510(k) clearance on 2022-03-07, under approval number K211639.

What company makes BTL-785W?

BTL-785W is manufactured by BTL Industries, Inc..

What is the FDA product code for BTL-785W?

The FDA product code for BTL-785W 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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