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

DIAG FAST-CATH DUO & TRIO REMOVABLE HEMOSTASIS ADAPTERS W/SIDEPORTS & 3-WAY STOPCOCKS

K Number: K954317 · Decision Nov 28, 1995
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
63
Review Days
74

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Basic Information

Device Name
DIAG FAST-CATH DUO & TRIO REMOVABLE HEMOSTASIS ADAPTERS W/SIDEPORTS & 3-WAY STOPCOCKS
K Number
K954317
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Daig Corp.
Date Received
September 15, 1995
Decision Date
November 28, 1995
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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K964518 FAST-CATH TRANSSEPTAL CATHETER INTRODUCER
K965249 SPYGLASS ANGIOGRAPHIC CATHETER
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K944284 CONTROL
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