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

MORSE VASCULAR INTRODUCER SET

K Number: K912961 · Decision Sep 11, 1991
Classifications
1
FEI Numbers
268
Registration Numbers
268
Same Product Code
682
Applicant Total
28
Review Days
65

Basic Information

Device Name
MORSE VASCULAR INTRODUCER SET
K Number
K912961
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
NORTH AMERICAN INSTRUMENT CORP.
Date Received
July 8, 1991
Decision Date
September 11, 1991
Product Code
DYB
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
DYB Introducer, Catheter

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