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510(k) FDA Premarket Notification K231434

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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
08435750411417 K231434 000
08435750415651 K231434 000
08435750415668 K231434 000
08435750415675 K231434 000
08435750415682 K231434 000
08435750415699 K231434 000
08435750415705 K231434 000
08435457265627 K231434 000
08435457265634 K231434 000
08435457265641 K231434 000
08435457265658 K231434 000
08435457265665 K231434 000
08435457265672 K231434 000
08435457272649 K231434 000
08435457272656 K231434 000
08435457273592 K231434 000
08435457280804 K231434 000
08435750415644 K231434 000
08435750415255 K231434 000
08435750413268 K231434 000
08435750414289 K231434 000
08435750414296 K231434 000
08435750414302 K231434 000
08435750414319 K231434 000
08435750414326 K231434 000
08435750414333 K231434 000
08435750414340 K231434 000
08435750414357 K231434 000
08435750414364 K231434 000
08435750414371 K231434 000
08435750415200 K231434 000
08435750415217 K231434 000
08435750415224 K231434 000
08435750415231 K231434 000
08435750415248 K231434 000
08435457282518 K231434 000
08435457273226 K231434 000
08435457273233 K231434 000
08435457273424 K231434 000
08435457273431 K231434 000
08435457273448 K231434 000
08435457273455 K231434 000
08435457273462 K231434 000
08435457273479 K231434 000
08435457273486 K231434 000
08435457273493 K231434 000
08435457273509 K231434 000
08435457273516 K231434 000
08435457273523 K231434 000
08435457273530 K231434 000
08435457273547 K231434 000
08435457273554 K231434 000
08435457273561 K231434 000
08435457273578 K231434 000
08435457273417 K231434 000
08435457273400 K231434 000
08435457273240 K231434 000
08435457273257 K231434 000
08435457273264 K231434 000
08435457273271 K231434 000
08435457273288 K231434 000
08435457273295 K231434 000
08435457273301 K231434 000
08435457273318 K231434 000
08435457273325 K231434 000
08435457273332 K231434 000
08435457273349 K231434 000
08435457273356 K231434 000
08435457273363 K231434 000
08435457273370 K231434 000
08435457273387 K231434 000
08435457273394 K231434 000
08435457273585 K231434 000

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Severity: Notice

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Filename: fda.report/pmn_item.php

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Backtrace:

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Line: 156
Function: _error_handler


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