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
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
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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