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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 5 of 5 Results
ProductCode: MSD Applicant: COVIDIEN Decision Date To: 03/29/2023
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Device Name
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510(K)
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palindrome precision h chronic catheter, palindrome precision si chronic catheter, palindrome precision hsi chronic cath COVIDIEN K123196 01/31/2013
palindrome h, si, hsi chronic catheter COVIDIEN K112477 09/28/2011
palindrome rt chronic catheter COVIDIEN K111817 08/30/2011
tal pallindrome (tm) symmetric tip dual lumen catheter, mahurkar (r) maxid (tm) dual lumen catheter, palindrome (tm)... COVIDIEN K111372 08/04/2011
palindrome p hemodialysis catheter COVIDIEN LP, FORMERLY REGISTERED AS KENDALL K092205 10/30/2009
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