510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K003576Substantially Equivalent

Q-Tel Rms (Rehabilitation Management System), Model 000503

Quinton, Inc., Bothell WA / Abbreviated, Substantially Equivalent
FDA source (opens on fda.gov)

K003576 is the FDA 510(k) clearance record for Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 000503, a class II device, cleared for Quinton, Inc. on under FDA product code DSI (Detector And Alarm, Arrhythmia). FDA records list 164 510(k) clearances for Quinton, Inc., from to . As of , FDA records show one recall naming K003576.

Clearance record

Decision date
Received
(66 days to decision)
Product code
DSI Detector And Alarm, Arrhythmia
Regulation
21 CFR 870.1025
Device class
Class II
Review panel
Cardiovascular
Applicant
Quinton, Inc. 3303 Monte Villa Pkwy., Bothell WA
510(k) summary
Summary
Third party review
No

Clearances, product code DSI

Trailing 12 months
1 clearance under product code DSI in the twelve months to October 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DSI, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260