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510(k) FDA Premarket Notification K233597

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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
00841517109240 K233597 000
00841517110673 K233597 000
00841517110666 K233597 000
00841517110659 K233597 000
00841517110642 K233597 000
00841517110635 K233597 000
00841517110628 K233597 000
00841517110611 K233597 000
00841517110604 K233597 000
00841517110789 K233597 000
00841517110765 K233597 000
00841517110758 K233597 000
00841517110802 K233597 000
00841517110727 K233597 000
00841517110253 K233597 000
00841517110031 K233597 000
00841517110024 K233597 000
00841517110185 K233597 000
00841517110178 K233597 000
00841517110192 K233597 000
00841517100018 K233597 000
00841517110598 K233597 000
00841517110314 K233597 000
00841517110307 K233597 000
00841517110291 K233597 000
00841517110246 K233597 000
00841517110321 K233597 000
00841517110796 K233597 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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