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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: KXA
Date Received: 12/27/1993
Decision Date: 02/03/1995
Decision: 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: KXA
Date Received: 12/27/1993
Decision Date: 02/03/1995
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
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