FDA 510(k) Application Details - K241270

Device Classification Name Powered Laser Surgical Instrument

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510(K) Number K241270
Device Name Powered Laser Surgical Instrument
Applicant BTL Industries, Inc.
362 Elm Street
Marlborough, MA 01752 US
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Contact David Chmel
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Regulation Number 878.4810

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Classification Product Code GEX
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Date Received 05/06/2024
Decision Date 01/30/2025
Decision SESE - SUBST EQUIV
Classification Advisory Committee SU - General & Plastic Surgery
Review Advisory Committee SU - General & Plastic Surgery
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review

FDA Source Information for K241270


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