510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K970764Substantially Equivalent

Comeg Endoscopy Resectoscope Accessories

Comeg Endoscopy, Aurora CO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K970764 is the FDA 510(k) clearance record for COMEG ENDOSCOPY RESECTOSCOPE ACCESSORIES, a class II device, cleared for Comeg Endoscopy on under FDA product code OCX (Endoscopic Irrigation/Suction System). FDA's definition for product code OCX reads: "To supply sterile water, other solutions and/or suction to endoscopes during endoscopic procedures". FDA records list 3 510(k) clearances for Comeg Endoscopy, from to . As of , FDA records show no recalls naming K970764.

Clearance record

Decision date
Received
(50 days to decision)
Product code
OCX Endoscopic Irrigation/Suction System
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Comeg Endoscopy 13790 E. Rice Pl., Aurora CO
510(k) summary
Summary
Third party review
No

Clearances, product code OCX

Trailing 12 months

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

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