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510(k) FDA Premarket Notification K240430

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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
05060396173660 K240430 000
05060396173295 K240430 000
05060396173288 K240430 000
05060396173271 K240430 000
05060396173264 K240430 000
05060396173257 K240430 000
05060396173240 K240430 000
05060396173233 K240430 000
05060396173226 K240430 000
05060396173219 K240430 000
05060396173202 K240430 000
05060396173196 K240430 000
05060396173189 K240430 000
05060396173097 K240430 000
05060396173066 K240430 000
05060396172380 K240430 000
05060396172373 K240430 000
05060396173301 K240430 000
05060396173363 K240430 000
05060396173370 K240430 000
05060396173639 K240430 000
05060396173622 K240430 000
05060396173615 K240430 000
05060396173608 K240430 000
05060396173585 K240430 000
05060396173578 K240430 000
05060396173561 K240430 000
05060396173554 K240430 000
05060396173547 K240430 000
05060396173516 K240430 000
05060396173455 K240430 000
05060396173448 K240430 000
05060396173431 K240430 000
05060396173400 K240430 000
05060396173394 K240430 000
05060396173387 K240430 000
05060396173592 K240430 000

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Line: 156
Function: _error_handler

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