510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K833421Substantially Equivalent

Programmable Stimulator 2352

Medtronic, Inc., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K833421 is the FDA 510(k) clearance record for PROGRAMMABLE STIMULATOR 2352, a class II device, cleared for Medtronic Vascular on under FDA product code JOQ (Generator, Pulse, Pacemaker, External Programmable (For Electrophysiological Studies Only)). FDA records list 1,525 510(k) clearances for Medtronic, Inc., from to . As of , FDA records show no recalls naming K833421.

Clearance record

Decision date
Received
(119 days to decision)
Product code
JOQ Generator, Pulse, Pacemaker, External Programmable (For Electrophysiological Studies Only)
Regulation
21 CFR 870.1750
Device class
Class II
Review panel
Cardiovascular
Applicant
Medtronic Vascular 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code JOQ

Trailing 12 months

FDA records hold no clearances under product code JOQ in the trailing twelve months.

FDA records show no clearances under product code JOQ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code JOQ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260