510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K993041Substantially Equivalent

Olympus Xcyf-1T3 Oes Cystofiberscope/nephrofiberscope Accessories and Ancillary Equipment

Olympus Optical Co., Ltd., West Cadwell NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K993041 is the FDA 510(k) clearance record for OLYMPUS XCYF-1T3 OES CYSTOFIBERSCOPE/NEPHROFIBERSCOPE ACCESSORIES AND ANCILLARY EQUIPMENT, a class II device, cleared for The Olympus Optical Co. on under FDA product code FAJ (Cystoscope And Accessories, Flexible/Rigid). FDA's definition for product code FAJ reads: "To examine and perform procedures within the urinary tract. For reusable, flexible endoscopes in this product code, validated reprocessing instructions and reprocessing validation data must be included in a 510(k) submission (82 FR 26807...". FDA records list 48 510(k) clearances for The Olympus Optical Co., from to . As of , FDA records show one recall naming K993041.

Clearance record

Decision date
Received
(202 days to decision)
Product code
FAJ Cystoscope And Accessories, Flexible/Rigid
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
The Olympus Optical Co. 1129 Bloomfield Ave., West Cadwell NJ
510(k) summary
Summary
Third party review
No

Clearances, product code FAJ

Trailing 12 months
5 clearances under product code FAJ in the twelve months to October 2026, April 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code FAJ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20262
May 20262
June 20260
July 20260
August 20260
September 20260
October 20260