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

IMPRA DUAL LUMEN SUBCLAVIAN CATHETER

K Number: K872163 · Decision Oct 30, 1987
Classifications
1
FEI Numbers
271
Registration Numbers
272
Same Product Code
880
Applicant Total
29
Review Days
147

Basic Information

Device Name
IMPRA DUAL LUMEN SUBCLAVIAN CATHETER
K Number
K872163
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
IMPRA, INC.
Date Received
June 5, 1987
Decision Date
October 30, 1987
Product Code
DQY
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
DQY Catheter, Percutaneous

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K983769 DISTAFLO BYPASS GRAFT
K983861 DISTAFLO BYPASS GRAFT
K983064 IMPRA HIGH POROSITY GRAFT
K981079 VENAFLO PTFE VASCULAR GRAFT, VENAFLO GRAFT WITH CARBON, VENAFLO VASCULAR GRAFT
K981076 VENAFLO PTFE VASCULAR GRAFT, VENAFLO GRAFT WITH CARBON, VENAFLO VASCULAR GRAFT
K971192 IMPRA EPTFE ARTERIOVENOUS CUFFED GRAFT
K964877 IMPRA EPTFE ARTERIOVENOUS CUFFED GRAFT
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