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510(k) FDA Premarket Notification K233744

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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
B648C43428091381 K233744 000
B648C33426090701 K233744 000
B648C33426090601 K233744 000
B648C33422091201 K233744 000
B648C33422091101 K233744 000
B648C33422091001 K233744 000
B648C33422090901 K233744 000
B648C33422090801 K233744 000
B648C33422090701 K233744 000
B648C33426090801 K233744 000
B648C33426090901 K233744 000
B648C33426091001 K233744 000
B648C43428091281 K233744 000
B648C43428091181 K233744 000
B648C43428091081 K233744 000
B648C43428090981 K233744 000
B648C43428090881 K233744 000
B648C43428090781 K233744 000
B648C33426091201 K233744 000
B648C33426091101 K233744 000
B648C33422090601 K233744 000

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Line: 156
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