510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K841347Substantially Equivalent

Laryngeal Stent

E. Benson Hood Laboratories, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K841347 is the FDA 510(k) clearance record for LARYNGEAL STENT, a class II device, cleared for E. Benson Hood Laboratories, Inc. on under FDA product code FWN (Prosthesis, Larynx (Stents And Keels)). FDA records list 6 510(k) clearances for E. Benson Hood Laboratories, Inc., from to . As of , FDA records show no recalls naming K841347.

Clearance record

Decision date
Received
(30 days to decision)
Product code
FWN Prosthesis, Larynx (Stents And Keels)
Regulation
21 CFR 874.3620
Device class
Class II
Review panel
Ear, Nose, Throat
Applicant
E. Benson Hood Laboratories, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code FWN

Trailing 12 months

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

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