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

Sniper Infusion Catheter with Balloon Occlusion

K Number: K180904 · Decision Jun 8, 2018
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
89
Applicant Total
3
Review Days
63

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Basic Information

Device Name
Sniper Infusion Catheter with Balloon Occlusion
K Number
K180904
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4450
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Embolx, Inc.
Date Received
April 6, 2018
Decision Date
June 8, 2018
Product Code
MJN
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
Y

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MJN Catheter, Intravascular Occluding, Temporary

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MJN), ordered by most recent decision date.

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Other Clearances by Embolx, Inc.

K Number Device Name
K232536 Soldier Microcatheter
K142692 Occlusion Balloon Catheter