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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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