FDA 510(k), K121712, AIRSTRIP RPM FOR LIFENET CONSULT

FDA 510(k), K121712, AIRSTRIP RPM FOR LIFENET CONSULT

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510(K) Number: K121712
Device Name: AIRSTRIP RPM FOR LIFENET CONSULT
Manufacturer: ROBERT A MILLER
Device Classification Name: System, Network And Communication, Physiological Monitors
Regulation Number: MSX
Classification Product Code: 06/11/2012
Date Received: 11/20/2012
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular

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