FDA 510(k), K936108, MASTERSCREEN BODY
FDA 510(k), K936108, MASTERSCREEN BODY
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510(K) Number: K936108
Device Name: MASTERSCREEN BODY
Manufacturer: V.D. GROTHER
Device Classification Name: Plethysmograph, Volume
Regulation Number: JEH
Classification Product Code: 12/27/1993
Date Received: 02/03/1995
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
Device Name: MASTERSCREEN BODY
Manufacturer: V.D. GROTHER
Device Classification Name: Plethysmograph, Volume
Regulation Number: JEH
Classification Product Code: 12/27/1993
Date Received: 02/03/1995
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
- 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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