510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K933436Substantially Equivalent

Frame, Spectacle

Aoyama Optical Co., Ltd., Sabae-City, Fukui-Pref., JP / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K933436 is the FDA 510(k) clearance record for FRAME, SPECTACLE, a class I device, cleared for Aoyama Optical Co., Ltd. on under FDA product code HQZ (Frame, Spectacle). FDA records list one 510(k) clearance for Aoyama Optical Co., Ltd. As of , FDA records show no recalls naming K933436.

Clearance record

Decision date
Received
(58 days to decision)
Product code
HQZ Frame, Spectacle
Regulation
21 CFR 886.5842
Device class
Class I
Review panel
Ophthalmic
Applicant
Aoyama Optical Co., Ltd. 2-3-30, Kaminaka-Cho, Sabae-City, Fukui-Pref., JP
510(k) summary
Statement
Third party review
No

Clearances, product code HQZ

Trailing 12 months

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

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