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

SCI MED TUBING CONNECTORS

K Number: K831261 · Decision Jun 3, 1983
Classifications
1
FEI Numbers
149
Registration Numbers
150
Same Product Code
137
Applicant Total
109
Review Days
46

Basic Information

Device Name
SCI MED TUBING CONNECTORS
K Number
K831261
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4290
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
SCIMED LIFE SYSTEMS, INC.
Date Received
April 18, 1983
Decision Date
June 3, 1983
Product Code
DTL
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
DTL Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass

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K974684 SCIMED 7 FRENCH WISEGUIDE GUIDE CATHETER
K973945 LUGE GUIDE WIRE
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K964551 CHOICE SUPER SUPPORT PTCA GUIDE WIRE, CHOICE PLUS SUPER SUPPORT PTCA GUIDE WIRE, CHOICE EXCHANGE SUPER SUPPORT PTCA GUID
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