510(k) K920063

DISETRONIC DOLOMAT PUMP by Disetronic Medical Systems — Product Code FRW

K920063 is an FDA 510(k) premarket notification submitted by Disetronic Medical Systems for the device "DISETRONIC DOLOMAT PUMP". The FDA issued a decision of Substantially Equivalent on August 3, 1993. The device falls under product code FRW (Scale, Patient), a Class I device regulated under 21 CFR 880.2720. Disetronic Medical Systems has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 3, 1993
Date Received
January 7, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Scale, Patient
Device Class
Class I
Regulation Number
880.2720
Review Panel
HO
Submission Type