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

INFUSION PUMP #6202

K Number: K771478 · Decision Aug 22, 1977
Classifications
1
FEI Numbers
149
Registration Numbers
149
Same Product Code
847
Applicant Total
16
Review Days
18

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
INFUSION PUMP #6202
K Number
K771478
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Roche Medical Electronics, Inc.
Date Received
August 4, 1977
Decision Date
August 22, 1977
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FRN), ordered by most recent decision date.

View all

Other Clearances by Roche Medical Electronics, Inc.

K Number Device Name
K791559 ROCHE SENSOR ADAPTOR
K791038 FETASONDE UTERINE ACTIVITY MONITOR
K791036 FETASONDE UTERINE WORK MONITOR
K791037 FETASONDE LABOR STATUS DISPLAY
K791035 FETASONDE FETAL ACTIVITY MONITOR
K791039 FETASONDE FETAL HEART RATE VARIABILITY
K790761 FETASONDE MODEL 2108
K790421 ROCHE LACTATE ANALYZER 640
K782088 MONITOR, HEART RATE MODEL 105
K782089 MONITOR, HEART RATE MODEL 103
Search all 16 clearances from Roche Medical Electronics, Inc. →