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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