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

ABD VARISOFT STEERABLE GUIDE WIRE AND ABD VARISOFT GUIDE WIRE EXTENSION

K Number: K981936 · Decision Feb 16, 2000
Classifications
1
FEI Numbers
257
Registration Numbers
258
Same Product Code
763
Applicant Total
1
Review Days
624

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Basic Information

Device Name
ABD VARISOFT STEERABLE GUIDE WIRE AND ABD VARISOFT GUIDE WIRE EXTENSION
K Number
K981936
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1330
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Advanced Biomedical Devices, Inc.
Date Received
June 2, 1998
Decision Date
February 16, 2000
Product Code
DQX
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
DQX Wire, Guide, Catheter

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