510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K935590Substantially Equivalent

Ep Medical, Inc. Ep-3 Clinical Stimulator

Ep Medical, Inc., Budd Lake NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K935590 is the FDA 510(k) clearance record for EP MEDICAL, INC. EP-3 CLINICAL STIMULATOR, a class II device, cleared for Ep Medical, Inc. on under FDA product code JOQ (Generator, Pulse, Pacemaker, External Programmable (For Electrophysiological Studies Only)). FDA records list 3 510(k) clearances for Ep Medical, Inc., from to . As of , FDA records show no recalls naming K935590.

Clearance record

Decision date
Received
(168 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
Ep Medical, Inc. 58 Rte. 46 W., Budd Lake NJ
510(k) summary
Statement
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