510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K963120Substantially Equivalent

Responder 2500 Defibrillator and Cardiac Care System

Marquette Electronics, Inc., Milwaukee WI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K963120 is the FDA 510(k) clearance record for RESPONDER 2500 DEFIBRILLATOR AND CARDIAC CARE SYSTEM, a class II device, cleared for Marquette Electronics, Inc. on under FDA product code DRO (Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)). FDA records list 82 510(k) clearances for Marquette Electronics, Inc., from to . As of , FDA records show no recalls naming K963120.

Clearance record

Decision date
Received
(200 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
Marquette Electronics, Inc. 8200 W. Tower Ave., Milwaukee WI
510(k) summary
Summary
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