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
K811180Substantially Equivalent

Ultramatic Project-O-Chart Ophth. Proj

American Optical Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K811180 is the FDA 510(k) clearance record for ULTRAMATIC PROJECT-O-CHART OPHTH. PROJ, a class I device, cleared for American Optical Corp. on under FDA product code HOS (Projector, Ophthalmic). FDA records list 35 510(k) clearances for American Optical Corp., from to . As of , FDA records show no recalls naming K811180.

Clearance record

Decision date
Received
(17 days to decision)
Product code
HOS Projector, Ophthalmic
Regulation
21 CFR 886.1680
Device class
Class I
Review panel
Ophthalmic
Applicant
American Optical Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code HOS

Trailing 12 months

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

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