FDA 510(k) Application Details - K241169

Device Classification Name Tubes, Gastrointestinal (And Accessories)

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510(K) Number K241169
Device Name Tubes, Gastrointestinal (And Accessories)
Applicant Gravitas Medical, Inc.
2332 Fourth St.
Suite E
Berkeley, CA 94710 US
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Contact Saheel Sutaria
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Regulation Number 876.5980

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Classification Product Code KNT
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Date Received 04/26/2024
Decision Date 11/22/2024
Decision SESE - SUBST EQUIV
Classification Advisory Committee GU - Gastroenterology & Urology
Review Advisory Committee GU - Gastroenterology & Urology
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review

FDA Source Information for K241169


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