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FDA 510(k) Applications for Medical Device Product Code "PCF"
FDA 510(k) Number
Applicant
Device Name
Decision Date
K122658
FEMASYS INC.
FEMCERV ENDOCERVICAL SAMPLER MODEL 3 SIZES: REF FCV-013, REF FCV-011, REF FCV-009
12/20/2012
K060320
FEMSPEC L.L.C.
FEMECC ENDOCERVICAL CURETTE
07/28/2006
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