510(k) K151560

Device
QuickPlan
Applicant
Siris Medical
510(k) number
K151560
Product code
MUJ  
Decision
Substantially Equivalent (SESE)
Decision date
2015-09-11
Date received
2015-06-10
Regulation
892.5050
Classification name
System, Planning, Radiation Therapy Treatment
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Colin M Carpenter
Address
257 Castro St., Suite 224 Mountain View CA US 94041 94041

FDA Registration Numbers

Source Documents

510(k) summary PDF

Related GUDID Devices

Primary DIBrandCompanyPublished
B244ISS100S0InsightRT Software Suite ServerSIRIS MEDICAL, INC.2016-08-08
B244IRT1000InsightRTSIRIS MEDICAL, INC.2016-08-08

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Legacy Summary

summary

FDA Review

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