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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