Cleared Traditional

K821067 - VIVONEX ACUTROL ENTERNAL FEEDING SYS

K821067 is an FDA 510(k) clearance for VIVONEX ACUTROL ENTERNAL FEEDING SYS, manufactured by Norwich Eaton Pharmaceuticals, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code KNT cleared through the Traditional 510(k) pathway after a 13-day FDA review.

K821067 · Norwich Eaton Pharmaceuticals, Inc. · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Apr 1982
Decision
13d
Days
Class 2
Risk

K821067 is an FDA 510(k) clearance for the VIVONEX ACUTROL ENTERNAL FEEDING SYS. Classified as Tubes, Gastrointestinal (and Accessories) (product code KNT), Class II - Special Controls.

Submitted by Norwich Eaton Pharmaceuticals, Inc. (Mchenry, US). The FDA issued a Cleared decision on April 29, 1982 after a review of 13 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5980 - the FDA gastroenterology and urology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

FDA 510(k) Submission Details - K821067

510(k) Number K821067 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 16, 1982
Decision Date April 29, 1982
Days to Decision 13 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
118d faster than avg
Panel avg: 131d · This submission: 13d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KNT Device Classification - Class 2, Special Controls

Product Code KNT Tubes, Gastrointestinal (and Accessories)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5980
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Gastroenterology & Urology devices follow this clearance model.

Regulatory Peers - KNT Tubes, Gastrointestinal (and Accessories)

All 527
Devices cleared under the same product code (KNT) and FDA review panel - the closest regulatory comparables to K821067.
CONPHAR SILICONE FEEDING TUBE
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K821409 · Corpak Co. · May 1982
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ENTERNAL SOLUTION ADMIN. SET
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AM. PH. STERILE FEEDING TUBE
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ARGYLE PVC FEEDING TUBE
K820441 · Sherwood Medical Co. · Mar 1982