510(k) K253409

Device
C320LBB Delivery System (C320LBBS45), C320LBB Delivery System (C320LBBS48), C320LBB Delivery System (C320LBBL45), C320LBB Delivery System (C320LBBL48)
Applicant
Medtronic, Inc.
510(k) number
K253409
Product code
DQY
Decision
Substantially Equivalent (SESE)
Decision date
2025-12-19
Date received
2025-09-30
Regulation
870.1250
Classification name
Catheter, Percutaneous
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Ryan Peterfeso
Address
8200 Coral Sea St. N.E Mounds View MN US 55112 55112

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

Related GUDID Devices

Primary DIBrandCompanyPublished
00763000747480NAMEDTRONIC, INC.2026-02-09
00763000747473NAMEDTRONIC, INC.2026-02-09
00763000747466NAMEDTRONIC, INC.2026-02-09
00763000747459NAMEDTRONIC, INC.2026-02-09

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