FLOOR MOUNT TUBESTAND-PERFORMER-N 6610.102/S-9110

System, X-ray, Stationary

CONTINENTAL X-RAY CORP.

The following data is part of a premarket notification filed by Continental X-ray Corp. with the FDA for Floor Mount Tubestand-performer-n 6610.102/s-9110.

Pre-market Notification Details

Device IDK912515
510k NumberK912515
Device Name:FLOOR MOUNT TUBESTAND-PERFORMER-N 6610.102/S-9110
ClassificationSystem, X-ray, Stationary
Applicant CONTINENTAL X-RAY CORP. 2000 SOUTH 25TH AVE. Broadview,  IL  60153
ContactOscar Khutoryansky
CorrespondentOscar Khutoryansky
CONTINENTAL X-RAY CORP. 2000 SOUTH 25TH AVE. Broadview,  IL  60153
Product CodeKPR  
CFR Regulation Number892.1680 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1991-06-06
Decision Date1991-09-19

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