510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K962850Substantially Equivalent

Tum-E-Vac

Ethox Corp., Buffalo NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K962850 is the FDA 510(k) clearance record for TUM-E-VAC, a class II device, cleared for Ethox Corp. on under FDA product code KDH (Catheter (Gastric, Colonic, Etc.), Irrigation And Aspiration). FDA records list 9 510(k) clearances for Ethox Corp., from to . As of , FDA records show no recalls naming K962850.

Clearance record

Decision date
Received
(214 days to decision)
Product code
KDH Catheter (Gastric, Colonic, Etc.), Irrigation And Aspiration
Regulation
21 CFR 876.5980
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Ethox Corp. 251 Seneca St., Buffalo NY
510(k) summary
Summary
Third party review
No

Clearances, product code KDH

Trailing 12 months

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

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