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

ITC GUIDING CATHETER

K Number: K913052 · Decision Nov 22, 1991
Classifications
1
FEI Numbers
271
Registration Numbers
272
Same Product Code
880
Applicant Total
28
Review Days
136

Basic Information

Device Name
ITC GUIDING CATHETER
K Number
K913052
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
INTERVENTIONAL THERAPEUTICS CORP.
Date Received
July 9, 1991
Decision Date
November 22, 1991
Product Code
DQY
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
DQY Catheter, Percutaneous

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