Cleared Traditional

K830119 - NEEDLE CATHETER JEJUNOSTOMY KIT

K830119 is the FDA 510(k) clearance for NEEDLE CATHETER JEJUNOSTOMY KIT by Biosearch Medical Products, Inc.. It is a Class 2 Gastroenterology & Urology device (product code KNT) cleared through the Traditional 510(k) pathway after a 17-day FDA review.

K830119 · Biosearch Medical Products, Inc. · Gastroenterology & Urology device
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Jan 1983
Decision
17d
Days
Class 2
Risk

K830119 is an FDA 510(k) clearance for the NEEDLE CATHETER JEJUNOSTOMY KIT. Classified as Tubes, Gastrointestinal (and Accessories) (product code KNT), Class II - Special Controls.

Submitted by Biosearch Medical Products, Inc. (Mchenry, US). The FDA issued a Cleared decision on January 28, 1983 after a review of 17 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.

View all Biosearch Medical Products, Inc. devices

Submission Details

510(k) Number K830119 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 11, 1983
Decision Date January 28, 1983
Days to Decision 17 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
113d faster than avg
Panel avg: 130d · This submission: 17d
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 257
Devices cleared under the same product code (KNT) and FDA review panel - the closest regulatory comparables to K830119.
ENTERAL DELIVERY SET
K831168 · Biosearch Medical Products, Inc. · May 1983
TOP-FILL BAG
K831169 · Biosearch Medical Products, Inc. · Apr 1983
ARGYLE SILICONE SALEM SUMP TUBE
K830710 · Sherwood Medical Co. · Mar 1983
TRAVASORB NASOGASTRIC NASOINTESTINAL
K823082 · Travenol Laboratories, S.A. · Nov 1982
FACE SHIELDS
K822004 · Kelleher Corp. · Oct 1982
PEDI-TUBE PEDIATRIC FEEDING TUBE
K822875 · Biosearch Medical Products, Inc. · Oct 1982