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FDA 510(k), K960224, GERATHERM MERCUIRY FREE CLINICAL THERMOMETER
FDA 510(k), K960224, GERATHERM MERCUIRY FREE CLINICAL THERMOMETER
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510(K) Number: K960224
Device Name: GERATHERM MERCUIRY FREE CLINICAL THERMOMETER
Manufacturer: RG ENT., INC.
Device Classification Name: Thermometer, Clinical Mercury
Regulation Number: 880.2920
Classification Product Code: FLK
Date Received: 01/17/1996
Decision Date: 03/25/1996
Regulation Medical Specialty: General Hospital
Device Name: GERATHERM MERCUIRY FREE CLINICAL THERMOMETER
Manufacturer: RG ENT., INC.
Device Classification Name: Thermometer, Clinical Mercury
Regulation Number: 880.2920
Classification Product Code: FLK
Date Received: 01/17/1996
Decision Date: 03/25/1996
Regulation Medical Specialty: General Hospital
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- 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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