Cleared Traditional

K791714 - SURGIFEED

K791714 is the FDA 510(k) clearance for SURGIFEED by Health Development Corp.. It is a Class 2 Gastroenterology & Urology device (product code KNT) cleared through the Traditional 510(k) pathway after a 139-day FDA review.

K791714 · Health Development Corp. · Gastroenterology & Urology device
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Jan 1980
Decision
139d
Days
Class 2
Risk

K791714 is an FDA 510(k) clearance for the SURGIFEED. Classified as Tubes, Gastrointestinal (and Accessories) (product code KNT), Class II - Special Controls.

Submitted by Health Development Corp. (Mchenry, US). The FDA issued a Cleared decision on January 16, 1980 after a review of 139 days - within the typical 510(k) review window.

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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Gastroenterology & Urology review framework, consistent with the majority of Class II 510(k) submissions.

View all Health Development Corp. devices

Submission Details

510(k) Number K791714 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 30, 1979
Decision Date January 16, 1980
Days to Decision 139 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
9d slower than avg
Panel avg: 130d · This submission: 139d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 289
Devices cleared under the same product code (KNT) and FDA review panel - the closest regulatory comparables to K791714.
ENTERIC FEEDING TUBE W/SEGM. FLEX. WT.
K801558 · Biosearch Medical Products, Inc. · Jul 1980
ENTERAL & NASOGASTRIC SOL. ADMIN. SET
K800815 · G.D. Searle and Co. · Jul 1980
TUBE FEEDING CONTAINER 1500 ML DISPOSE.
K800955 · The Healthcare Group Laboratories, Inc. · May 1980
CONPHAR STOMACH TUBE-STERILE-X-RAY
K791250 · Conphar, Inc. · Aug 1979
CONPHAR FEEDING TUBE-STERILE
K791257 · Conphar, Inc. · Aug 1979
CONPHAR RECTAL TUBE-STERILE
K791268 · Conphar, Inc. · Aug 1979