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

XVAC

K Number: K110782 · Decision Apr 7, 2011
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
194
Applicant Total
61
Review Days
17

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Basic Information

Device Name
XVAC
K Number
K110782
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5830
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sorin Group Italia S.R.L.
Date Received
March 21, 2011
Decision Date
April 7, 2011
Product Code
CAC
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
CAC Apparatus, Autotransfusion

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Other Clearances by Sorin Group Italia S.R.L.

K Number Device Name
K253671 Dual Stage Venous Cannulae
K251783 Inspire HCR and HCR DUAL cardiotomy reservoirs
K253616 ProtekDilate Vascular Access Kit
K250610 Easyflow (103-200; 103-300); Easyflow Duo (103-210; 103-310)
K250150 VANGUARD Blood cardioplegia Systems (Vanguard 4:1 Blood cardioplegia set); VANGUARD Blood cardioplegia Systems (Vanguard 4:1 Blood cardioplegia set with shunt); VANGUARD Blood cardioplegia Systems (Vanguard 4:1 Blood Cardioplegia Set Mini)
K243264 DHF 0.2 Hemoconcentrator (DHF 02); DHF 0.6 Hemoconcentrator (DHF 06); SH 14 Hemoconcentrator (SH 14)
K242953 KIDS Arterial Filters
K242092 MICRO Arterial Filters
K241236 XTRA Collection sets; XTRA Sequestration set X
K240584 XTRA Autotransfusion System (with XTRA Bowl sets)
Search all 61 clearances from Sorin Group Italia S.R.L. →