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510(k) FDA Premarket Notification K242509

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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
00840314193636 K242509 000
00840314193469 K242509 000
00840314193452 K242509 000
00840314193445 K242509 000
00840314193438 K242509 000
00840314193421 K242509 000
00840314193414 K242509 000
00840314193407 K242509 000
00840314193391 K242509 000
00840314193384 K242509 000
00840314193377 K242509 000
00840314193360 K242509 000
00840314193353 K242509 000
00840314193346 K242509 000
00840314193339 K242509 000
00840314193476 K242509 000
00840314193483 K242509 000
00840314193629 K242509 000
00840314193612 K242509 000
00840314193605 K242509 000
00840314193599 K242509 000
00840314193582 K242509 000
00840314193575 K242509 000
00840314193568 K242509 000
00840314193551 K242509 000
00840314193544 K242509 000
00840314193537 K242509 000
00840314193520 K242509 000
00840314193513 K242509 000
00840314193506 K242509 000
00840314193490 K242509 000
00840314193322 K242509 000

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Message: Undefined index: deviceName

Filename: fda.report/pmn_item.php

Line Number: 156

Backtrace:

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Line: 156
Function: _error_handler

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