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510(k) FDA Premarket Notification K252582

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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
D745701188COM01150 K252582 000
D745701161COM00200 K252582 000
D745701161COM00180 K252582 000
D745701161COM00170 K252582 000
D745701161COM00160 K252582 000
D745701161COM00140 K252582 000
D745701161COM00130 K252582 000
D745701161COM00120 K252582 000
D745701161COM00100 K252582 000
D745701161COM00090 K252582 000
D745701161COM00080 K252582 000
D745701161COM00060 K252582 000
D745701161COM00050 K252582 000
D745701161COM00040 K252582 000
D745701161COM00020 K252582 000
D745701161COM00290 K252582 000
D745701161COM00300 K252582 000
D745701188COM01130 K252582 000
D745701188COM01120 K252582 000
D745701188COM01070 K252582 000
D745701188COM01040 K252582 000
D745701188COM01030 K252582 000
D745701188COM01020 K252582 000
D745701188COM01010 K252582 000
D745701188COM01000 K252582 000
D745701161COM00500 K252582 000
D745701161COM00480 K252582 000
D745701161COM00470 K252582 000
D745701161COM00440 K252582 000
D745701161COM00420 K252582 000
D745701161COM00410 K252582 000
D745701161COM00010 K252582 000

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Line: 156
Function: _error_handler


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