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

ARROW BIPOLAR PACING/BALLOON WEDGE PRESSURE CATHETER

K Number: K960479 · Decision Oct 17, 1996
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
127
Applicant Total
110
Review Days
258

Basic Information

Device Name
ARROW BIPOLAR PACING/BALLOON WEDGE PRESSURE CATHETER
K Number
K960479
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.3680
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ARROW INTL., INC.
Date Received
February 2, 1996
Decision Date
October 17, 1996
Product Code
LDF
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
LDF Electrode, Pacemaker, Temporary

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K071491 ARROW INTERNATIONAL, INC., SURGICAL DRAPES
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K041153 SHARPSAWAY II LOCKING DISPOSABLE CUP
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