510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K822169Substantially Equivalent

Surgical Head Support

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

K822169 is the FDA 510(k) clearance record for SURGICAL HEAD SUPPORT, a class I device, cleared for Kelleher Corp. on under FDA product code HBM (Headrest, Neurosurgical). FDA records list 94 510(k) clearances for Kelleher Corp., from to . As of , FDA records show no recalls naming K822169.

Clearance record

Decision date
Received
(28 days to decision)
Product code
HBM Headrest, Neurosurgical
Regulation
21 CFR 882.4440
Device class
Class I
Review panel
Neurology
Applicant
Kelleher Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code HBM

Trailing 12 months

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

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