FDA 510(k) Applications Submitted by SEDATELEC

FDA 510(k) Number Submission Date Device Name Applicant
K983798 10/28/1998 SEDATELEC ASP ACUPUNCTURE NEEDLES SEDATELEC
K983800 10/28/1998 DN ACUPUNTURE NEEDLES SEDATELEC
K060392 02/15/2006 ASP TITANIUM SEDATELEC
K101267 05/05/2010 PREMIO 10 MOXA SEDATELEC


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