510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K932773Substantially Equivalent

Frames, Spectacles

Diaco, Inc., Miami FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K932773 is the FDA 510(k) clearance record for FRAMES, SPECTACLES, a class I device, cleared for Diaco, Inc. on under FDA product code HQZ (Frame, Spectacle). FDA records list one 510(k) clearance for Diaco, Inc. As of , FDA records show no recalls naming K932773.

Clearance record

Decision date
Received
(104 days to decision)
Product code
HQZ Frame, Spectacle
Regulation
21 CFR 886.5842
Device class
Class I
Review panel
Ophthalmic
Applicant
Diaco, Inc. 5050 NW 74th Ave., Miami FL
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