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
K090326Substantially Equivalent

Ret Cam II, Retcam 3 and Retcam Shuttle and Portable Ophthalmic Imaging Systems

Clarity Medical Systems, Pleasanton CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K090326 is the FDA 510(k) clearance record for RET CAM II, RETCAM 3 AND RETCAM SHUTTLE AND PORTABLE OPHTHALMIC IMAGING SYSTEMS, a class II device, cleared for Clarity Medical Systems on under FDA product code HKI (Camera, Ophthalmic, Ac-Powered). FDA records list 4 510(k) clearances for Clarity Medical Systems, from to . As of , FDA records show 2 recalls naming K090326.

Clearance record

Decision date
Received
(289 days to decision)
Product code
HKI Camera, Ophthalmic, Ac-Powered
Regulation
21 CFR 886.1120
Device class
Class II
Review panel
Ophthalmic
Applicant
Clarity Medical Systems 5775 W. Las Positas Blvd., Pleasanton CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HKI

Trailing 12 months
3 clearances under product code HKI in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code HKI, trailing twelve months
MonthClearances
November 20250
December 20251
January 20261
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20260
October 20260