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Seigla Medical, Inc. FDA Approvals

0 new drug approvals and 2 device clearances on file. This applicant is not matched to a listed company.

Newest first

A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.

Product
LiquID .051 LP Guide Catheter Extension510(k)Apr 4, 2025Cardiovascular
LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension510(k)May 5, 2022Cardiovascular

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