510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K992703Substantially Equivalent

Cardiotron EKG Multi-Phase Information Analysis System, Models 3800, 6800, 8800

Premier Heart, LLC, Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K992703 is the FDA 510(k) clearance record for CARDIOTRON EKG MULTI-PHASE INFORMATION ANALYSIS SYSTEM, MODELS 3800, 6800, 8800, a class II device, cleared for Premier Heart, LLC on under FDA product code DQK (Computer, Diagnostic, Programmable). FDA records list one 510(k) clearance for Premier Heart, LLC. As of , FDA records show no recalls naming K992703.

Clearance record

Decision date
Received
(222 days to decision)
Product code
DQK Computer, Diagnostic, Programmable
Regulation
21 CFR 870.1425
Device class
Class II
Review panel
Cardiovascular
Applicant
Premier Heart, LLC 601 13th St., NW, Washington DC
510(k) summary
Summary
Third party review
No

Clearances, product code DQK

Trailing 12 months
25 clearances under product code DQK in the twelve months to October 2026, February 2026 the highest month at 5.
Show the numbers
Monthly 510(k) clearances under FDA product code DQK, trailing twelve months
MonthClearances
November 20250
December 20254
January 20262
February 20265
March 20260
April 20263
May 20261
June 20263
July 20264
August 20262
September 20261
October 20260