510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K811911Substantially Equivalent

Single Channel Non-Fade Oscilloscope

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

K811911 is the FDA 510(k) clearance record for SINGLE CHANNEL NON-FADE OSCILLOSCOPE, a class II device, cleared for Quinton, Inc. on under FDA product code DXJ (Display, Cathode-Ray Tube, Medical). FDA records list 164 510(k) clearances for Quinton, Inc., from to . As of , FDA records show no recalls naming K811911.

Clearance record

Decision date
Received
(27 days to decision)
Product code
DXJ Display, Cathode-Ray Tube, Medical
Regulation
21 CFR 870.2450
Device class
Class II
Review panel
Cardiovascular
Applicant
Quinton, 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