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510(k) FDA Premarket Notification K241605

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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
00814216028556 K241605 000
00814216028389 K241605 000
00814216028372 K241605 000
00814216028365 K241605 000
00814216028358 K241605 000
00814216028341 K241605 000
00814216028334 K241605 000
00814216028327 K241605 000
00814216028310 K241605 000
00814216028303 K241605 000
00814216028297 K241605 000
00814216028280 K241605 000
00814216028273 K241605 000
00814216028266 K241605 000
00814216028259 K241605 000
00814216028396 K241605 000
00814216028402 K241605 000
00814216028549 K241605 000
00814216028532 K241605 000
00814216028525 K241605 000
00814216028518 K241605 000
00814216028501 K241605 000
00814216028495 K241605 000
00814216028488 K241605 000
00814216028471 K241605 000
00814216028464 K241605 000
00814216028457 K241605 000
00814216028440 K241605 000
00814216028433 K241605 000
00814216028426 K241605 000
00814216028419 K241605 000
00814216028242 K241605 000

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Filename: fda.report/pmn_item.php

Line Number: 156

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Line: 156
Function: _error_handler

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