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FDA 510(k)

BTL-703

K-Number: K182363 · 2019-01-24

ApplicantBTL Industries, Inc.
Decision Date2019-01-24
Product CodeIMJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BTL-703 is a medical device manufactured by BTL Industries, Inc.. It received FDA 510(k) clearance on 2019-01-24 under approval number K182363. The device is classified under product code IMJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BTL-703?

BTL-703 is a medical device that received FDA 510(k) clearance on 2019-01-24. It is manufactured by BTL Industries, Inc.. The 510(k) number is K182363.

When was BTL-703 approved by the FDA?

BTL-703 received FDA 510(k) clearance on 2019-01-24, under approval number K182363.

What company makes BTL-703?

BTL-703 is manufactured by BTL Industries, Inc..

What is the FDA product code for BTL-703?

The FDA product code for BTL-703 is IMJ.

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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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