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510(k) FDA Premarket Notification K241164

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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
03613720286462 K241164 000
03613720286318 K241164 000
03613720286301 K241164 000
03613720286295 K241164 000
03613720286288 K241164 000
03613720286271 K241164 000
03613720286264 K241164 000
03613720286257 K241164 000
03613720286240 K241164 000
03613720286233 K241164 000
03613720286226 K241164 000
03613720286219 K241164 000
03613720286325 K241164 000
03613720286332 K241164 000
03613720286349 K241164 000
03613720286455 K241164 000
03613720286448 K241164 000
03613720286431 K241164 000
03613720286424 K241164 000
03613720286417 K241164 000
03613720286400 K241164 000
03613720286394 K241164 000
03613720286387 K241164 000
03613720286370 K241164 000
03613720286363 K241164 000
03613720286356 K241164 000
03613720286202 K241164 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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