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FDA 510(k) Applications Submitted by KATHERINE CO
FDA 510(k) Number
Submission Date
Device Name
Applicant
K011789
06/08/2001
PROCEDURE MASKS: PM4-301 AND PM4-304
PRIMELINE MEDICAL PRODUCTS, INC.
K001951
06/27/2000
PRIMED PLEATED TIE-BACK, PROCEDURE MASK PM4-305, PRIMED PLEATED EAR-LOOP, PROCEDURE MASK PM4-306
PRIMELINE MEDICAL PRODUCTS, INC.
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