OMNI DIAGNOST

Table, Radiographic, Tilting

XRE CORP.

The following data is part of a premarket notification filed by Xre Corp. with the FDA for Omni Diagnost.

Pre-market Notification Details

Device IDK874113
510k NumberK874113
Device Name:OMNI DIAGNOST
ClassificationTable, Radiographic, Tilting
Applicant XRE CORP. 300 FOSTER ST. Littleton,  MA  01460
ContactThomas F Flynn
CorrespondentThomas F Flynn
XRE CORP. 300 FOSTER ST. Littleton,  MA  01460
Product CodeIXR  
CFR Regulation Number892.1980 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1987-10-09
Decision Date1987-11-16

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