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

BETA I PROGRAMMABLE INFUSION PUMP

K Number: K831897 · Decision Aug 12, 1983
Classifications
1
FEI Numbers
149
Registration Numbers
149
Same Product Code
847
Applicant Total
12
Review Days
59

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Basic Information

Device Name
BETA I PROGRAMMABLE INFUSION PUMP
K Number
K831897
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Orange Medical Instruments, Inc.
Date Received
June 14, 1983
Decision Date
August 12, 1983
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 Orange Medical Instruments, Inc.

K Number Device Name
K860808 CONTINUCATH
K851822 BETA SCAN TRENDS METER
K844796 MICRO-BETA U100 SYRINGE
K843882 TRENDS LANCET
K841369 BETA SCAN DRYSTIX
K833705 BETAJECT BD U100
K833706 CLICK-COUNT U100 INSULIN SYRINGE
K832691 BETA SCAN REAGENT STRIP
K832793 NEOCATH 1000 W/HEPCOTE
K831523 BETA SCAN NORMAL CONTROL SOLUTION
Search all 12 clearances from Orange Medical Instruments, Inc. →