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

RM3 RENAL PRESERVATION SYSTEM--CONTROL UNIT

K Number: K971571 · Decision Jul 29, 1997
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
42
Applicant Total
12
Review Days
90

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
RM3 RENAL PRESERVATION SYSTEM--CONTROL UNIT
K Number
K971571
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5880
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Waters Instruments, Inc.
Date Received
April 30, 1997
Decision Date
July 29, 1997
Product Code
KDN
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
KDN System, Perfusion, Kidney

Similar 510(k) Clearances

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

View all

Other Clearances by Waters Instruments, Inc.

K Number Device Name
K053169 RM3 RENAL PRESERVATION SYSTEM
K042224 RM3 RENAL PRESERVATION SYSTEM
K921519 OXICOM-2100
K911207 OXICOMPLUS
K863210 VELCOM-100
K862161 OSC-80 OXIMETER
K852909 MVP - 6000
K834408 TX-2 THERMAL DILUTION CARDIAC OUTPUT
K841876 POLYURETHANE THERMAL DILUTION CATHET
K813585 WATERS ILEOSTOMY VALVE
Search all 12 clearances from Waters Instruments, Inc. →