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510(k) FDA Premarket Notification P000053

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The following data is part of a premarket notification filed by with the FDA for .

Pre-market Notification Details

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Correspondent

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
00878953000718 P000053 000
00878953000824 P000053 000
00878953000817 P000053 000
00878953000800 P000053 000
00878953000794 P000053 000
00878953000787 P000053 000
00878953000770 P000053 000
00878953000763 P000053 000
00878953000756 P000053 000
00878953000749 P000053 000
00878953000732 P000053 000
00878953004938 P000053 000
00878953005461 P000053 000
00878953000725 P000053 000
00878953000619 P000053 000
00878953000626 P000053 000
00878953000633 P000053 000
00878953000688 P000053 000
00878953003085 P000053 005
00878953003092 P000053 005
00878953003191 P000053 005
00878953003184 P000053 005
00878953003177 P000053 005
00878953003160 P000053 005
00878953003153 P000053 005
00878953003146 P000053 005
00878953003139 P000053 005
00878953003122 P000053 005
00878953003115 P000053 005
00878953003108 P000053 005
00878953003078 P000053 005
00878953005652 P000053 024

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