510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K760697Substantially Equivalent

Evans Arm and Hand Rest

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

K760697 is the FDA 510(k) clearance record for EVANS ARM AND HAND REST, a class I device, cleared for Alcon Laboratories on under FDA product code HRK (Table, Instrument, Manual, Ophthalmic). FDA records list 152 510(k) clearances for Alcon Laboratories, from to . As of , FDA records show no recalls naming K760697.

Clearance record

Decision date
Received
(41 days to decision)
Product code
HRK Table, Instrument, Manual, Ophthalmic
Regulation
21 CFR 886.4855
Device class
Class I
Review panel
Ophthalmic
Applicant
Alcon Laboratories 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code HRK

Trailing 12 months

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

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