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510(k) FDA Premarket Notification P050039

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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
10885862027078 P050039 000
10885862025289 P050039 000
10885862025296 P050039 000
10885862025302 P050039 000
10885862025319 P050039 000
10885862279026 P050039 000
10885862279033 P050039 000
10885862279040 P050039 000
10885862279057 P050039 000
10885862025272 P050039 000
10885862025265 P050039 000
10885862025258 P050039 000
10885862027139 P050039 000
10885862027207 P050039 000
10885862027214 P050039 000
10885862027221 P050039 000
10885862025210 P050039 000
10885862025227 P050039 000
10885862025234 P050039 000
10885862025241 P050039 000
10885862279064 P050039 000
10885862279071 P050039 000
10885862026026 P050039 000
10885862026033 P050039 000
10885862026040 P050039 000
10885862026057 P050039 000
10885862026361 P050039 000
10885862026422 P050039 000
10885862026484 P050039 000
10885862026491 P050039 000
10885862026019 P050039 000
10885862026002 P050039 000
10885862025999 P050039 000
10885862279088 P050039 000
10885862279095 P050039 000
10885862279101 P050039 000
10885862279118 P050039 000
10885862279125 P050039 000
10885862025968 P050039 000
10885862025975 P050039 000
10885862025982 P050039 000
10885862026507 P050039 000

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