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510(k) FDA Premarket Notification K082630

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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
10607411930598 K082630 000
00607411913624 K082630 000
00607411913631 K082630 000
00607411913648 K082630 000
00607411913655 K082630 000
00607411913662 K082630 000
00607411913679 K082630 000
00607411914997 K082630 000
00607411915017 K082630 000
00607411915079 K082630 000
00607411915086 K082630 000
00607411915093 K082630 000
00607411915123 K082630 000
00607411913617 K082630 000
00607411913600 K082630 000
10607411931991 K082630 000
10607411933766 K082630 000
10607411933902 K082630 000
00607411912733 K082630 000
00607411913518 K082630 000
00607411913525 K082630 000
00607411913532 K082630 000
00607411913549 K082630 000
00607411913563 K082630 000
00607411913570 K082630 000
00607411913587 K082630 000
00607411913594 K082630 000
00607411915130 K082630 000
00607411915154 K082630 000
00607411915178 K082630 000
00607411932168 K082630 000
00607411932267 K082630 000
00607411932328 K082630 000
00607411933721 K082630 000
10607411933797 K082630 000
10607411933933 K082630 000
00607411940408 K082630 000
00607411940491 K082630 000
10607411940566 K082630 000
10607411940573 K082630 000
10607411940580 K082630 000
00607411940729 K082630 000
00607411932083 K082630 000
10607411932011 K082630 000
00607411916458 K082630 000
00607411920264 K082630 000
00607411920271 K082630 000
00607411920288 K082630 000
00607411928772 K082630 000
00607411930447 K082630 000
00607411930454 K082630 000
00607411930461 K082630 000
00607411930546 K082630 000
00607411930607 K082630 000
00607411930614 K082630 000
10607411930628 K082630 000
10607411961066 K082630 000

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Filename: fda.report/pmn_item.php

Line Number: 156

Backtrace:

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Line: 156
Function: _error_handler


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