510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K033989Substantially Equivalent

Medtronic Selectsite Deflectable Catheter System, Models C304-S59 and C304-L69

Medtronic Inc. Cardiac Rhythm Management, Minneapolis MN / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K033989 is the FDA 510(k) clearance record for MEDTRONIC SELECTSITE DEFLECTABLE CATHETER SYSTEM, MODELS C304-S59 AND C304-L69, a class II device, cleared for Medtronic Inc. Cardiac Rhythm Management on under FDA product code DQY (Catheter, Percutaneous). FDA records list 2 510(k) clearances for Medtronic Inc. Cardiac Rhythm Management, from to . As of , FDA records show no recalls naming K033989.

Clearance record

Decision date
Received
(30 days to decision)
Product code
DQY Catheter, Percutaneous
Regulation
21 CFR 870.1250
Device class
Class II
Review panel
Cardiovascular
Applicant
Medtronic Inc. Cardiac Rhythm Management 7000 Central Ave., NE, Minneapolis MN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DQY

Trailing 12 months
13 clearances under product code DQY in the twelve months to October 2026, July 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code DQY, trailing twelve months
MonthClearances
November 20250
December 20252
January 20260
February 20260
March 20261
April 20262
May 20260
June 20262
July 20263
August 20262
September 20261
October 20260