UROSKOP C

System, X-ray, Stationary

SIEMENS CORP.

The following data is part of a premarket notification filed by Siemens Corp. with the FDA for Uroskop C.

Pre-market Notification Details

Device IDK811807
510k NumberK811807
Device Name:UROSKOP C
ClassificationSystem, X-ray, Stationary
Applicant SIEMENS CORP. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeKPR  
CFR Regulation Number892.1680 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1981-06-25
Decision Date1981-08-10

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