Opto Circuits India Ltd has informed that the Company has received 510(k) approval from Food and Drug Administration USA (US FDA) for the new generation Pluse Oximeters model no M30 and M34, which would enable the Company to market these Pluse Oximeters in United States of America (USA).
The Model 34 can store data in memory for later review and documentation and also features a sleep mode for basic patient sleep screening. It also enables the data transfer through USB / IRDA.
November 7, 2007
Opto Circuits gets USFDA for Pluse Oximeters
at 9:57 PM
Labels: Opto Circuits India
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