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FDA 510(k), K120412, 3M SPOTON TEMPERATURE MONITORING SYSTEM
FDA 510(k), K120412, 3M SPOTON TEMPERATURE MONITORING SYSTEM
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510(K) Number: K120412
Device Name: 3M SPOTON TEMPERATURE MONITORING SYSTEM
Manufacturer: ARIZANT HEALTHCARE INC.
Device Classification Name: thermometer, electronic, clinical
Regulation Number: 880.2910
Classification Product Code: FLL
Date Received: 02/10/2012
Decision Date: 05/30/2012
Regulation Medical Specialty: General Hospital
Device Name: 3M SPOTON TEMPERATURE MONITORING SYSTEM
Manufacturer: ARIZANT HEALTHCARE INC.
Device Classification Name: thermometer, electronic, clinical
Regulation Number: 880.2910
Classification Product Code: FLL
Date Received: 02/10/2012
Decision Date: 05/30/2012
Regulation Medical Specialty: General Hospital
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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