CORPAK FARRELL VALVE ENTERAL GASTRIC PRESSURE RELI— 510(k) K853253

Name: FDA 510(k) clearance K853253
Creator: U.S. Food and Drug Administration
Published: 1985-11-05

Substantially Equivalent

Corpak Co.

FDA 510(k) clearance K853253 for CORPAK FARRELL VALVE ENTERAL GASTRIC PRESSURE RELI, Substantially Equivalent on 1985-11-05. Applicant: Corpak Co.. Device class: 2.

Clearance details

Applicant: Corpak Co.
Product code: Code KNT
Device class: Class 2
Regulation: 21 CFR 876.5980
Advisory panel: Gastroenterology, Urology
Date received: 1985-08-02
Decision date: 1985-11-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wheeling, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KNT

view all

K261890 — 52Fr ViSiGi LUX; 52Fr ViSiGi 3D®2026-08-14
K253514 — Minnesota Four-Lumen Esophagogastric Tamponade Tube - 18 French (0092220) +2 more2026-07-10
K250389 — XNY Disposable Gastric Calibration Tube2025-04-10
K243228 — Flexi-Seal AIR (with ENFit Connector)2025-03-28
K242336 — hygh-tec Drainage II2025-01-17

More clearances from Corpak Co.

view all

K935512 — CORPAK REPLACEMENT GASTROSTOMY DEVICE STOMACORE1996-08-29
K931921 — CORPAK GASTROSTOMY TUBE1995-06-09
K932847 — CORPAK ENTERAL PUMP1994-06-17
K902949 — CORPAK GRASPING FORCEPS1990-08-30
K901501 — CORPAK GASTROSTOMY TUBE1990-06-11

Adverse events under product code KNT

product code KNT

Death: 192
Injury: 6,034
Malfunction: 4,049
Other: 1
Total: 10,276

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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