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510(k) FDA Premarket Notification K240690

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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
00889929055762 K240690 000
00889929055151 K240690 000
00889929055144 K240690 000
00889929055137 K240690 000
00889929055120 K240690 000
00889929055113 K240690 000
00889929055106 K240690 000
00889929055090 K240690 000
00889929055083 K240690 000
00889929055076 K240690 000
00889929055069 K240690 000
00889929055052 K240690 000
00889929055045 K240690 000
00889929055038 K240690 000
00889929055021 K240690 000
00889929055960 K240690 000
00889929055168 K240690 000
00889929055175 K240690 000
00889929055182 K240690 000
00889929055755 K240690 000
00889929055748 K240690 000
00889929055731 K240690 000
00889929055724 K240690 000
00889929055717 K240690 000
00889929055557 K240690 000
00889929055540 K240690 000
00889929055533 K240690 000
00889929055304 K240690 000
00889929055298 K240690 000
00889929055281 K240690 000
00889929055274 K240690 000
00889929055267 K240690 000
00889929055250 K240690 000
00889929055199 K240690 000
00889929057971 K240690 000

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Filename: fda.report/pmn_item.php

Line Number: 156

Backtrace:

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Line: 156
Function: _error_handler

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