510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K203226Substantially Equivalent

Telescope 0 O 10Mm Wl 305Mm / Telescope 30 O 10Mm Wl 305Mm / Telescope 50 O 10Mm Wl 305Mm, Telescope 0 O 10Mm Wl 440Mm / Telescope 30 O 10Mm Wl 440Mm / Telescope 50 O 10Mm Wl 440Mm

Richard Wolf Medical Instruments Corp., Vernon Hills IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K203226 is the FDA 510(k) clearance record for TELESCOPE 0 O 10MM WL 305MM / TELESCOPE 30 O 10MM WL 305MM / TELESCOPE 50 O 10MM WL 305MM, TELESCOPE 0 O 10MM WL 440MM / TELESCOPE 30 O 10MM WL 440MM / TELESCOPE 50 O 10MM WL 440MM, a class II device, cleared for Richard Wolf Medical Instruments Corporation on under FDA product code GCM (Endoscope, Rigid). FDA records list 153 510(k) clearances for Richard Wolf Medical Instruments Corporation, from to . As of , FDA records show no recalls naming K203226.

Clearance record

Decision date
Received
(193 days to decision)
Product code
GCM Endoscope, Rigid
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Richard Wolf Medical Instruments Corporation 353 Corporate Woods Pkwy., Vernon Hills IL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GCM

Trailing 12 months

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

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