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

RIVER PUMP

K Number: K932895 · Decision Mar 31, 1994
Classifications
1
FEI Numbers
149
Registration Numbers
149
Same Product Code
847
Applicant Total
16
Review Days
290

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Basic Information

Device Name
RIVER PUMP
K Number
K932895
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
River Medical, Inc.
Date Received
June 14, 1993
Decision Date
March 31, 1994
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 River Medical, Inc.

K Number Device Name
K023174 DISPOSABLE TEMPORARY PACING WIRE
K944351 SMARTDOSE IV PREFILLED INFUSION CONTAINER
K944352 SMARTDOSE III INFUSION CONTAINER
K945298 SMARTFLOW I ADMINISTRATION SET
K943692 SMART DOSE(TM)
K933335 RIVER VIAL ADAPTER
K915120 TEF/PLATINUM PISTON
K915121 TEF/WIRE PISTON
K913287 H/A PARTIAL - REGULAR & H/A PARTIAL - OFFSET
K913285 PTFE PISTON
Search all 16 clearances from River Medical, Inc. →