510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K871611Substantially Equivalent

Allergan Humphrey Auto-Refractor, Models 525 & 540

Allergan Humphrey, San Leandro CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K871611 is the FDA 510(k) clearance record for ALLERGAN HUMPHREY AUTO-REFRACTOR, MODELS 525 & 540, a class I device, cleared for Allergan Humphrey on under FDA product code HKO (Refractometer, Ophthalmic). FDA records list 3 510(k) clearances for Allergan Humphrey, from to . As of , FDA records show no recalls naming K871611.

Clearance record

Decision date
Received
(38 days to decision)
Product code
HKO Refractometer, Ophthalmic
Regulation
21 CFR 886.1760
Device class
Class I
Review panel
Ophthalmic
Applicant
Allergan Humphrey 3081 Teagarden St., San Leandro CA
Third party review
No

Clearances, product code HKO

Trailing 12 months

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

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