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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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