510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K840353Substantially Equivalent

Pacemaker Pulse Generator W/electrode

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

K840353 is the FDA 510(k) clearance record for PACEMAKER PULSE GENERATOR W/ELECTRODE, a class II device, cleared for Ross Research, Inc. on under FDA product code DRO (Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)). FDA records list 2 510(k) clearances for Ross Research, Inc., from to . As of , FDA records show no recalls naming K840353.

Clearance record

Decision date
Received
(88 days to decision)
Product code
DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
Regulation
21 CFR 870.5550
Device class
Class II
Review panel
Cardiovascular
Applicant
Ross Research, Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code DRO

Trailing 12 months

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

FDA records show no clearances under product code DRO in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DRO, 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