510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K000905Substantially Equivalent

Urethrotome 8667.Xxx and 8670.Xxx

Richard Wolf Medical Instruments Corp., Vernon Hills IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K000905 is the FDA 510(k) clearance record for URETHROTOME 8667.XXX AND 8670.XXX, a class II device, cleared for Richard Wolf Medical Instruments Corp. on under FDA product code EZO (Urethrotome). FDA records list 153 510(k) clearances for Richard Wolf Medical Instruments Corp., from to . As of , FDA records show no recalls naming K000905.

Clearance record

Decision date
Received
(52 days to decision)
Product code
EZO Urethrotome
Regulation
21 CFR 876.4770
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Richard Wolf Medical Instruments Corp. 353 Corporate Woods Pkwy., Vernon Hills IL
510(k) summary
Summary
Third party review
No

Clearances, product code EZO

Trailing 12 months

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

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