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

CORREC TORR TM

K Number: K813137 · Decision Dec 2, 1981
Classifications
1
FEI Numbers
87
Registration Numbers
87
Same Product Code
147
Applicant Total
39
Review Days
27

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Basic Information

Device Name
CORREC TORR TM
K Number
K813137
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2850
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Norton Performance Plastics Corp.
Date Received
November 5, 1981
Decision Date
December 2, 1981
Product Code
DRS
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
DRS Transducer, Blood-Pressure, Extravascular

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K851299 CORRECT FLO
K842858 FLUID ADMINISTRATION LINE W/SPIKE 14-923
K841828 CENTRAL VENOUS CATHETER W/BIG-GARD
K840240 MICROFUSE INTRAVENOUS CATHETER SET
K831587 TEMP. REPAIR KIT-DUAL LUMEN CATHETER
K831698 DISPOSABLE PRESSURE TRANSDUCER#14004195
K830788 CENTRAL VEIN CATHERIZATION KIT-14-690-
K830813 FRENCH PERCUTANEOUS SHEATH INTRODUCER
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