FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DISETRONIC PANOMAT PUMP

K Number: K915566 · Decision Aug 7, 1992
Classifications
1
FEI Numbers
149
Registration Numbers
149
Same Product Code
847
Applicant Total
17
Review Days
239

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Basic Information

Device Name
DISETRONIC PANOMAT PUMP
K Number
K915566
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Disetronic Medical Systems
Date Received
December 12, 1991
Decision Date
August 7, 1992
Product Code
FRN
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FRN Pump, Infusion

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Other Clearances by Disetronic Medical Systems

K Number Device Name
K013782 DISETRONIC PENFINE INSULIN INJECTION PEN NEEDLE
K994186 DISETRONIC D-TRON INSULIN INFUSION PUMP
K994197 DISENTRONIC PENFINE INJECTION PEN NEEDLE
K993666 DISETRONIC PEN P100
K991376 DAHEDI INSULIN INFUSION PUMP
K990259 DISETRONIC MULTIFUSE INFUSION PUMP SYSTEM
K982966 DISETRONIC PEN
K982399 DISETRONIC PENFINE INJECTION PEN NEEDLE
K973339 DISETRONIC PENFINE INJECTION PEN NEEDLE
K973044 DISETRONIC H-TRON PLUS V 100 INSULIN INFUSION PUMP
Search all 17 clearances from Disetronic Medical Systems →