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

PE-01 ELECTRONIC INFUSION PUMP

K Number: K812898 · Decision Dec 2, 1981
Classifications
1
FEI Numbers
149
Registration Numbers
149
Same Product Code
847
Applicant Total
10
Review Days
47

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Basic Information

Device Name
PE-01 ELECTRONIC INFUSION PUMP
K Number
K812898
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Egnell, Inc.
Date Received
October 16, 1981
Decision Date
December 2, 1981
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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K840526 AMETHERM
K834335 AMEDA PHOTOTHERAPY LAMP FOR NEWBORN
K832637 AMEDA NEONATAL RESUSCITATION UNIT-
K813312 UNIVERSAL SUCTION PUMP TYPE EUS
K813095 GASTRIC JUICES SUCTION PUMP
K812020 EGNELL COMPACT, TYPE EHV