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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 IDP030035
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
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Combination ProductError Temporarily Unavailable Please Select Your Back Button Or Choose A Page Listed Below. Thank You.

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
05414734502948 P030035 001
H758PM311001 P030035 053
05414734503785 P030035 053
05414734507882 P030035 108
05414734507899 P030035 108
05414734507905 P030035 108
05414734507912 P030035 108
05414734509084 P030035 138
05414734509091 P030035 138
05414734510080 P030035 171
05414734510097 P030035 171

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