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

VELCOM-100

K Number: K863210 · Decision Nov 26, 1986
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
136
Applicant Total
12
Review Days
98

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Basic Information

Device Name
VELCOM-100
K Number
K863210
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2100
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Waters Instruments, Inc.
Date Received
August 20, 1986
Decision Date
November 26, 1986
Product Code
DPW
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DPW Flowmeter, Blood, Cardiovascular

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Other Clearances by Waters Instruments, Inc.

K Number Device Name
K053169 RM3 RENAL PRESERVATION SYSTEM
K042224 RM3 RENAL PRESERVATION SYSTEM
K971571 RM3 RENAL PRESERVATION SYSTEM--CONTROL UNIT
K921519 OXICOM-2100
K911207 OXICOMPLUS
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. →