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510(k) FDA Premarket Notification K233967

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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
10887587078502 K233967 000
10887587077192 K233967 000
10887587077208 K233967 000
10887587077215 K233967 000
10887587077390 K233967 000
10887587077406 K233967 000
10887587077413 K233967 000
10887587077420 K233967 000
10887587077437 K233967 000
10887587077178 K233967 000
10887587077161 K233967 000
10887587077147 K233967 000
10887587077055 K233967 000
10887587077062 K233967 000
10887587077079 K233967 000
10887587077086 K233967 000
10887587077093 K233967 000
10887587077109 K233967 000
10887587077123 K233967 000
10887587077130 K233967 000
10887587077444 K233967 000
10887587077451 K233967 000
07612334229816 K233967 000
07612334263513 K233967 000
07612334263520 K233967 000
07612334263537 K233967 000
07612334263544 K233967 000
07612334263483 K233967 000
07612334263452 K233967 000
07612334263469 K233967 000
07612334229809 K233967 000
07612334229793 K233967 000
07612334229786 K233967 000
10887587077468 K233967 000
10887587077475 K233967 000
10887587077482 K233967 000
10887587077499 K233967 000
10887587077505 K233967 000
10887587077512 K233967 000
10887587077529 K233967 000
10887587077536 K233967 000
07612334263476 K233967 000

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Function: _error_handler

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