TUM-E-VAC— 510(k) K962850

Substantially Equivalent

Ethox Corp.

FDA 510(k) clearance K962850 for TUM-E-VAC, Substantially Equivalent on 1997-02-21. Applicant: Ethox Corp.. Device class: 2.

Clearance details

Applicant: Ethox Corp.
Product code: Code KDH
Device class: Class 2
Regulation: 21 CFR 876.5980
Advisory panel: Gastroenterology, Urology
Date received: 1996-07-22
Decision date: 1997-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Buffalo, NY, US

Download summary PDF View on FDA.gov ↗

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K885220 — PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT1989-09-25

Data sourced from openFDA. This site is unofficial and independent of the FDA.