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510(k) FDA Premarket Notification P010015

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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
00885074200736 P010015 003
00885074200743 P010015 003
00885074200729 P010015 003
00613994308658 P010015 012
00885074113364 P010015 012
00885074113371 P010015 012
00613994753304 P010015 084
00613994713667 P010015 084
00643169351905 P010015 227
00643169590571 P010015 247
00643169590588 P010015 247
00643169590595 P010015 247
00643169735637 P010015 317
00643169735644 P010015 317
00643169735651 P010015 317
00643169735668 P010015 317
00643169735675 P010015 317
00643169735682 P010015 317
00643169891456 P010015 338
00643169891449 P010015 338
00643169891432 P010015 338
00643169891425 P010015 338
00643169891418 P010015 338
00643169891401 P010015 338
00763000002046 P010015 399

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