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

Vein Clamps, Artery Clamps

K Number: K161315 · Decision Aug 18, 2016
Classifications
1
FEI Numbers
186
Registration Numbers
186
Same Product Code
203
Applicant Total
1
Review Days
99

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Basic Information

Device Name
Vein Clamps, Artery Clamps
K Number
K161315
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.4450
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Aros Surgical Instruments Corporation
Date Received
May 11, 2016
Decision Date
August 18, 2016
Product Code
DXC
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
DXC Clamp, Vascular

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