510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K830899Substantially Equivalent

Three Channel Monitor Series 6700

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

K830899 is the FDA 510(k) clearance record for THREE CHANNEL MONITOR SERIES 6700, a class II device, cleared for Marquette Electronics, Inc. on under FDA product code DXJ (Display, Cathode-Ray Tube, Medical). FDA records list 82 510(k) clearances for Marquette Electronics, Inc., from to . As of , FDA records show no recalls naming K830899.

Clearance record

Decision date
Received
(22 days to decision)
Product code
DXJ Display, Cathode-Ray Tube, Medical
Regulation
21 CFR 870.2450
Device class
Class II
Review panel
Cardiovascular
Applicant
Marquette Electronics, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code DXJ

Trailing 12 months
1 clearance under product code DXJ in the twelve months to October 2026, September 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DXJ, 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 20261
October 20260