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

TCPM II TOURNIQUET CUFF PRESSURE MONITOR

K Number: K900104 · Decision Mar 15, 1990
Classifications
1
FEI Numbers
107
Registration Numbers
107
Same Product Code
33
Applicant Total
41
Review Days
65

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Basic Information

Device Name
TCPM II TOURNIQUET CUFF PRESSURE MONITOR
K Number
K900104
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.5910
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Electromedics, Inc.
Date Received
January 9, 1990
Decision Date
March 15, 1990
Product Code
KCY
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
KCY Tourniquet, Pneumatic

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K925412 ELECTROMEDICS TISSUE TRAP/ #TT280
K915737 AUTOTRANSFUSION BLOOD COLLECTION RESERVOIR
K910238 PORTABLE AUTO TRANSFUSION SYSTEM 500
K910935 MODIFIED PYROGEN TESTING
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