510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K842090Substantially Equivalent

Rhino-Larynx Stroboscope Type 4914

Bruel & Kjaer Industri A/S, Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K842090 is the FDA 510(k) clearance record for RHINO-LARYNX STROBOSCOPE TYPE 4914, a class I device, cleared for Bruel & Kjaer Industri A/S on under FDA product code EQL (Laryngostroboscope). FDA records list 4 510(k) clearances for Bruel & Kjaer Industri A/S, from to . As of , FDA records show no recalls naming K842090.

Clearance record

Decision date
Received
(55 days to decision)
Product code
EQL Laryngostroboscope
Regulation
21 CFR 874.4750
Device class
Class I
Review panel
Ear, Nose, Throat
Applicant
Bruel & Kjaer Industri A/S 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code EQL

Trailing 12 months

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

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