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

MVR COLLAPSIBLE VENOUS RESERVOIR BAG

K Number: K920774 · Decision Oct 19, 1992
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
168
Applicant Total
475
Review Days
242

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Basic Information

Device Name
MVR COLLAPSIBLE VENOUS RESERVOIR BAG
K Number
K920774
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4400
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtronic Vascular
Date Received
February 20, 1992
Decision Date
October 19, 1992
Product Code
DTN
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
DTN Reservoir, Blood, Cardiopulmonary Bypass

Similar 510(k) Clearances

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Other Clearances by Medtronic Vascular

K Number Device Name
K232570 Steerant™ Super Stiff Guidewire
K232190 6F Sherpa NX Balanced Guide Catheter, 7F Sherpa NX Balanced Guide Catheter
K230156 5F Launcher Guide Catheter, 6F Launcher Guide Catheter, 7F Launcher Guide Catheter, 8F Launcher Guide Catheter
K220773 Everest 20 Inflation Device and 3-way Stopcock (AC2200);Everest 30 Inflation Device and 3-way Stopcock (AC3200);Everest 20 Survival Kit containing:1. Everest 20 Device with 3-way Stopcock, 2. Piton Y-Adaptor ,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC2205P); Everest 30 Survival Kit containing:1. Everest 30 Device with 3-way Stopcock, 2. Piton Y-Adaptor,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC3205P)
K192296 Medtronic 6F Taiga Guiding Catheter
K173515 Admiral Xtreme
K162097 InTRAkit
K162027 TRAcelet Compression Device
K161287 DxTerity, DxTerity TRA, DxTerity Angio-Kit, DxTerity EZ-Pak, DxTerity TRA Angio-Kit, DxTerity TRA EZ-Pak
K133539 TOTAL ACROSS
Search all 475 clearances from Medtronic Vascular →