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510(k) FDA Premarket Notification P030022

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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
03596010194435 P030022 000
00885556020258 P030022 000
00885556020432 P030022 000
00885556020494 P030022 000
00885556021644 P030022 000
00885556021064 P030022 000
00885556021453 P030022 000
00885556021415 P030022 000
00885556021316 P030022 000
00885556021248 P030022 000
00885556021071 P030022 000
00885556021002 P030022 000
00885556020975 P030022 000
00885556020869 P030022 000
00885556020838 P030022 000
00885556020678 P030022 000
00885556020074 P030022 000
00885556019993 P030022 000
03596010194480 P030022 000
03596010194497 P030022 000
03596010194466 P030022 000
03596010194503 P030022 000
03596010194459 P030022 000
03596010194510 P030022 000
03596010194527 P030022 000
00885556019726 P030022 000
00885556019801 P030022 000
00885556019818 P030022 000
03596010194442 P030022 000
03596010194473 P030022 000
00885556020661 P030022 008
00885556020531 P030022 008
20885556028500 P030022 008
00885556019849 P030022 008
00885556020241 P030022 008
00885556020685 P030022 008
20885556028692 P030022 008
20885556028296 P030022 008
20885556027879 P030022 008
20885556027732 P030022 008
00885556027646 P030022 008
20885556027381 P030022 008
20885556027251 P030022 008
00885556022894 P030022 008
20885556026988 P030022 008
00885556021552 P030022 008
00885556021309 P030022 008
00885556021750 P030022 008
00885556021927 P030022 008
00885556022047 P030022 008
00885556022115 P030022 008
00885556022313 P030022 008
00885556274415 P030022 025
00885556274866 P030022 025
00885556274910 P030022 025
00885556274965 P030022 025
00885556281390 P030022 025
00885556281444 P030022 025

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Severity: Notice

Message: Undefined index: deviceName

Filename: fda.report/pmn_item.php

Line Number: 156

Backtrace:

File: /var/www/fda.report/pmn_item.php
Line: 156
Function: _error_handler


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