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510(k) FDA Premarket Notification K222623

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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
00850039704611 K222623 000
00850039704901 K222623 000
00850039704895 K222623 000
00850039704888 K222623 000
00850039704871 K222623 000
00850039704772 K222623 000
00850039704765 K222623 000
00850039704758 K222623 000
00850039704741 K222623 000
00850070544252 K222623 000
00850070544238 K222623 000
00850070544214 K222623 000
00850070544207 K222623 000
00850070544191 K222623 000
00850070544184 K222623 000
00850070544177 K222623 000
00850039704789 K222623 000
00850039704796 K222623 000
10850039704496 K222623 000
10850039704489 K222623 000
10850039704472 K222623 000
10850039704465 K222623 000
10850039704458 K222623 000
10850039704441 K222623 000
10850039704434 K222623 000
10850039704427 K222623 000
00850039704864 K222623 000
00850039704857 K222623 000
00850039704840 K222623 000
00850039704833 K222623 000
00850039704826 K222623 000
00850039704819 K222623 000
00850039704802 K222623 000
00850070544160 K222623 000

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