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

INSTRUMED VASCULAR CLAMPS

K Number: K092544 · Decision Oct 26, 2009
Classifications
1
FEI Numbers
186
Registration Numbers
186
Same Product Code
203
Applicant Total
7
Review Days
68

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Basic Information

Device Name
INSTRUMED VASCULAR CLAMPS
K Number
K092544
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4450
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Instrumed International, Inc.
Date Received
August 19, 2009
Decision Date
October 26, 2009
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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