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510(k) FDA Premarket Notification K232659

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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
30850054867064 K232659 000
30850054867316 K232659 000
30850054867286 K232659 000
30850054867279 K232659 000
30850054867262 K232659 000
30850054867255 K232659 000
30850054867248 K232659 000
30850054867231 K232659 000
30850054867224 K232659 000
30850054867675 K232659 000
30850054867668 K232659 000
30850054867651 K232659 000
30850054867644 K232659 000
30850054867637 K232659 000
30850054867620 K232659 000
30850054867606 K232659 000
30850054867590 K232659 000
30850054867576 K232659 000
00850054867841 K232659 000
30850054867903 K232659 000
30850065976601 K232659 000
30850065976564 K232659 000
30850065976168 K232659 000
30850065976151 K232659 000
30850065976137 K232659 000
30850065976120 K232659 000
30850065976113 K232659 000
30850065976106 K232659 000
30850065976052 K232659 000
00850065976044 K232659 000
30850065976021 K232659 000
30850065976007 K232659 000
30850054867989 K232659 000
30850054867941 K232659 000
30850054867934 K232659 000
30850054867927 K232659 000
30850054867910 K232659 000
30850054867507 K232659 000

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Filename: fda.report/pmn_item.php

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Line: 156
Function: _error_handler

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