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

ITC COAXIAL ANGIOGRAPHIC CATH SET, MODIFICATION

K Number: K912477 · Decision Nov 5, 1991
Classifications
1
FEI Numbers
213
Registration Numbers
214
Same Product Code
497
Applicant Total
28
Review Days
154

Basic Information

Device Name
ITC COAXIAL ANGIOGRAPHIC CATH SET, MODIFICATION
K Number
K912477
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1200
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
INTERVENTIONAL THERAPEUTICS CORP.
Date Received
June 4, 1991
Decision Date
November 5, 1991
Product Code
DQO
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
DQO Catheter, Intravascular, Diagnostic

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