FDA 510(k) Applications Submitted by KEYSTONE MEDICAL

FDA 510(k) Number Submission Date Device Name Applicant
K011860 06/14/2001 KEYST0NE MEDICAL PICC CATHETER KEYSTONE MEDICAL
K001958 06/27/2000 KEYSTONE MEDICAL SCHON XL SOFT-LINE DOUBLE LUMENT CATHETER. KEYSTONE MEDICAL 12 F DUO-FLOW AND 14F DUO-FLOW 400 XL CATH KEYSTONE MEDICAL


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