510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K822259Substantially Equivalent

Laryngeal Spatulas

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

K822259 is the FDA 510(k) clearance record for LARYNGEAL SPATULAS, a class I device, cleared for Kelleher Corp. on under FDA product code EQH (Source, Carrier, Fiberoptic Light). FDA records list 94 510(k) clearances for Kelleher Corp., from to . As of , FDA records show no recalls naming K822259.

Clearance record

Decision date
Received
(85 days to decision)
Product code
EQH Source, Carrier, Fiberoptic Light
Regulation
21 CFR 874.4350
Device class
Class I
Review panel
Ear, Nose, Throat
Applicant
Kelleher Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code EQH

Trailing 12 months

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

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