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

INTRODUCER, CAT. #INT-06FR.

K Number: K771041 · Decision Jul 13, 1977
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
69
Review Days
34

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Basic Information

Device Name
INTRODUCER, CAT. #INT-06FR.
K Number
K771041
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Sorensen Research
Date Received
June 9, 1977
Decision Date
July 13, 1977
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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