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Error Temporarily Unavailable Please Select Your Back Button Or Choose A Page Listed Below. Thank You.

Error Temporarily Unavailable Please Select Your Back Button Or Choose A Page Listed Below. Thank You.

The following data is part of a premarket notification filed by Error Temporarily Unavailable Please Select Your Back Button Or Choose A Page Listed Below. Thank You. with the FDA for Error Temporarily Unavailable Please Select Your Back Button Or Choose A Page Listed Below. Thank You..

Pre-market Notification Details

Device IDK222225
510k NumberError Temporarily Unavailable
Device Name:Error Temporarily Unavailable Please Select Your Back Button Or Choose A Page Listed Below. Thank You.
ClassificationError Temporarily Unavailable Please Select Your Back Button Or Choose A Page Listed Below. Thank You.
Applicant#Error.diagnostics#
ContactError Temporarily Unavailable Please Select Your Back Button Or Choose A Page Listed Below. Thank You.
CorrespondentError Temporarily Unavailable Please Select Your Back Button Or Choose A Page Listed Below. Thank You.
#Error.diagnostics#
Product CodeError Temporarily Unavailable Please Select Your Back Button Or Choose A Page Listed Below. Thank You.
CFR Regulation NumberError Temporarily Unavailable [🔎]
DecisionError Temporarily Unavailable Please Select Your Back Button Or Choose A Page Listed Below. Thank You.
TypeError Temporari
3rd Party ReviewedError Temporarily Unavailable Please Select Your Back Button Or Choose A Page Listed Below. Thank You.
Combination ProductError Temporarily Unavailable Please Select Your Back Button Or Choose A Page Listed Below. Thank You.

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
20860011916608 K222225 000
20860011820196 K222225 000
20860011820189 K222225 000
20860011820172 K222225 000
20860011820165 K222225 000

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