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510(k) FDA Premarket Notification K242833

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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
00822409130573 K242833 000
00822409130412 K242833 000
00822409130405 K242833 000
00822409130399 K242833 000
00822409130382 K242833 000
00822409130375 K242833 000
00822409130368 K242833 000
00822409130351 K242833 000
00822409130344 K242833 000
00822409130337 K242833 000
00822409130320 K242833 000
00822409130313 K242833 000
00822409130306 K242833 000
00822409130290 K242833 000
00822409130429 K242833 000
00822409130436 K242833 000
00822409130566 K242833 000
00822409130559 K242833 000
00822409130542 K242833 000
00822409130535 K242833 000
00822409130528 K242833 000
00822409130511 K242833 000
00822409130504 K242833 000
00822409130498 K242833 000
00822409130481 K242833 000
00822409130474 K242833 000
00822409130467 K242833 000
00822409130450 K242833 000
00822409130443 K242833 000
00822409130283 K242833 000

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