Devices

Device Recall Rita Thermopads

Model / Serial
Lot codes affected: Y110503-1 and Y103003-2. 510k number : k031926 Contract manufacturer, Katecho, Inc, registration number 1932007
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
No
Distribution
Product was shipped to 18 field representatives and 87 customers (hospitals and medical centers
Product Description
Dispersive Electrodes packaged in an 8x10 plastic container.
Manufacturer
Rita Medical Systems
1 Event
- Recall of Device Recall Rita Thermopads

Manufacturer

Rita Medical Systems

Manufacturer Address
Rita Medical Systems, 967 N Shoreline Blvd, Mountain View CA 94043-1932
Source
USFDA

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