510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K833538Substantially Equivalent

Dowing Ophthalmic Chair-Non/ac Power

Vision Health Technology, Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K833538 is the FDA 510(k) clearance record for DOWING OPHTHALMIC CHAIR-NON/AC POWER, a class I device, cleared for Vision Health Technology on under FDA product code HMD (Chair, Ophthalmic, Manual). FDA records list 3 510(k) clearances for Vision Health Technology, from to . As of , FDA records show no recalls naming K833538.

Clearance record

Decision date
Received
(152 days to decision)
Product code
HMD Chair, Ophthalmic, Manual
Regulation
21 CFR 886.1140
Device class
Class I
Review panel
Ophthalmic
Applicant
Vision Health Technology 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code HMD

Trailing 12 months

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

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