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
K943921Substantially Equivalent

Ryder Contact Lens Case

Clinical Research Assoc., Brunswick NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K943921 is the FDA 510(k) clearance record for RYDER CONTACT LENS CASE, a class II device, cleared for Clinical Research Assoc. on under FDA product code LRX (Case, Contact Lens). FDA records list one 510(k) clearance for Clinical Research Assoc. As of , FDA records show no recalls naming K943921.

Clearance record

Decision date
Received
(60 days to decision)
Product code
LRX Case, Contact Lens
Regulation
21 CFR 886.5928
Device class
Class II
Review panel
Ophthalmic
Applicant
Clinical Research Assoc. 1588 Rte. 130 N.,, Brunswick NJ
510(k) summary
Summary
Third party review
No

Clearances, product code LRX

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