FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

PRESSORE MONITOR

K Number: K954670 · Decision Oct 30, 1995
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
14
Applicant Total
8
Review Days
20

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Basic Information

Device Name
PRESSORE MONITOR
K Number
K954670
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.1615
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cleveland Medical Devices, Inc.
Date Received
October 10, 1995
Decision Date
October 30, 1995
Product Code
IKE
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
IKE Transducer, Miniature Pressure

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Other Clearances by Cleveland Medical Devices, Inc.

K Number Device Name
K063872 KINESIA
K042039 FAMILY OF CRYSTAL 20 MONITORS MODEL #CS20-600,900,1300,1400,2400 & 120
K013863 CRYSTAL MONITOR MODEL 16
K001110 CRYSTAL-EEG MODEL 15
K970672 CRYSTAL-EEG MODEL 10 (MODEL 10)
K964690 LIBERTY VALVE
K962591 FOOT WEIGHT ALARM