FDA.report

510(k) K932760

Device
DFS-2100
Applicant
DBA SYSTEMS, INC.
510(k) number
K932760
Product code
LMA  
Decision
Substantially Equivalent (SESE)
Decision date
1994-10-20
Date received
1993-06-08
Regulation
892.2030
Classification name
Digitizer, Image, Radiological
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
KENNETH CAMPBELL
Address
1200 S. Woody Burke Rd. Melbourne FL US 32902 32902

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF not indicated by FDA · openFDA JSON

Legacy Summary

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FDA Review

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