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

Guide Sheath

K Number: K190644 · Decision Apr 18, 2019
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
11
Review Days
36

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Basic Information

Device Name
Guide Sheath
K Number
K190644
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Surmodics,Inc.
Date Received
March 13, 2019
Decision Date
April 18, 2019
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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K Number Device Name
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K231828 Pounce™ Sheath
K231022 Pounce™ Thrombectomy System
K221886 Sublime Microcatheter
K220501 Pounce Thrombectomy System
K211492 Pounce Thrombectomy System
K192814 Pounce Thrombus Retrieval System
K173560 Microcatheter
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