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Sedatelec
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
3
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K101267
PREMIO 10 MOXA
December 3, 2010
K060392
ASP TITANIUM
April 26, 2006
K983798
SEDATELEC ASP ACUPUNCTURE NEEDLES
August 27, 1999
K983800
DN ACUPUNTURE NEEDLES
August 27, 1999