Cleared Traditional

K832103 - BLOOD TUBING SET

K832103 is an FDA 510(k) clearance for BLOOD TUBING SET, manufactured by Lee Medical Intl., Inc.. The device is a Class 2 Gastroenterology & Urology device with product code KOC cleared through the Traditional 510(k) pathway after a 50-day FDA review.

K832103 · Lee Medical Intl., Inc. · Gastroenterology & Urology device
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Aug 1983
Decision
50d
Days
Class 2
Risk

K832103 is an FDA 510(k) clearance for the BLOOD TUBING SET. Classified as Accessories, Blood Circuit, Hemodialysis (product code KOC), Class II - Special Controls.

Submitted by Lee Medical Intl., Inc. (Mchenry, US). The FDA issued a Cleared decision on August 12, 1983 after a review of 50 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5820 - 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 Lee Medical Intl., Inc. devices

FDA 510(k) Submission Details - K832103

510(k) Number K832103 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 23, 1983
Decision Date August 12, 1983
Days to Decision 50 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
81d faster than avg
Panel avg: 131d · This submission: 50d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KOC Device Classification - Class 2, Special Controls

Product Code KOC Accessories, Blood Circuit, Hemodialysis
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5820
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 - KOC Accessories, Blood Circuit, Hemodialysis

All 142
Devices cleared under the same product code (KOC) and FDA review panel - the closest regulatory comparables to K832103.
SINGLE PATIENT SYS. II MODEL DM-450
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TISSUE FORCEPS
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K832252 · Terumo Medical Corp. · Aug 1983
GF-180-L HOLLOW FIBER HEMODIALYSIS
K831606 · Gambro, Inc. · Jun 1983
CLIRANS TAF 120 HOLLOW FIBER DIALYZ. &
K831482 · Terumo Medical Corp. · Jun 1983
EXTRASENSR ULTRAFILTRATION MONITOR
K831433 · Extracorporeal Medical Specialities, Inc. · Jun 1983