FDA.report

510(k) K992693

Device
RITA MODEL 90 ELECTROSURGICAL ACCESSORY, MODEL 90
Applicant
RITA MEDICAL SYSTEMS
510(k) number
K992693
Product code
GEI  
Decision
Substantially Equivalent (SESE)
Decision date
1999-09-10
Date received
1999-08-12
Regulation
878.4400
Classification name
Electrosurgical, Cutting & Coagulation & Accessories
Medical specialty
General & Plastic Surgery
Review panel
General & Plastic Surgery
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
No
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
ERIN DIGNAN
Address
967 N. Shoreline Blvd. Mountain View CA US 94043 94043

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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Legacy Summary

summary

FDA Review

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