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510(k) FDA Premarket Notification K223825

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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
16971292000973 K223825 000
16971292006654 K223825 000
06971292006602 K223825 000
06971292006572 K223825 000
16971292006555 K223825 000
16971292002878 K223825 000
16971292002885 K223825 000
16971292003066 K223825 000
16971292003059 K223825 000
16971292003042 K223825 000
16971292003035 K223825 000
16971292003028 K223825 000
16971292003004 K223825 000
16971292002991 K223825 000
16971292002984 K223825 000
16971292002977 K223825 000
16971292002960 K223825 000
16973810850398 K223825 000
16971292006661 K223825 000
16971292006678 K223825 000
16971292006685 K223825 000
16971292000966 K223825 000
16971292000959 K223825 000
16971292000904 K223825 000
16971292000898 K223825 000
16971292000881 K223825 000
16971292000874 K223825 000
16973810850251 K223825 000
16973810850268 K223825 000
16973810850299 K223825 000
16973810850282 K223825 000
16973810850329 K223825 000
16973810850312 K223825 000
16971292000980 K223825 000
06971292006725 K223825 000
06971292006718 K223825 000
06971292006701 K223825 000
16971292006692 K223825 000
16971292003080 K223825 000

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Function: _error_handler

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