510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K862903Substantially Equivalent

Middle Ear Viewer and Fluid Collector

Steven K. Juhn, Minneapolis MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K862903 is the FDA 510(k) clearance record for MIDDLE EAR VIEWER AND FLUID COLLECTOR, a class I device, cleared for Steven K. Juhn on under FDA product code JZF (Tube, Ear Suction). FDA records list one 510(k) clearance for Steven K. Juhn. As of , FDA records show no recalls naming K862903.

Clearance record

Decision date
Received
(116 days to decision)
Product code
JZF Tube, Ear Suction
Regulation
21 CFR 874.4420
Device class
Class I
Review panel
Ear, Nose, Throat
Applicant
Steven K. Juhn Gutenkauf, Minneapolis MN
Third party review
No

Clearances, product code JZF

Trailing 12 months

FDA records hold no clearances under product code JZF in the trailing twelve months.

FDA records show no clearances under product code JZF in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code JZF, 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