Cleared Traditional

K872750 - LAKE CATHETER CARE KIT

K872750 is an FDA 510(k) clearance for LAKE CATHETER CARE KIT, manufactured by Lake Medical Products, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code KOD cleared through the Traditional 510(k) pathway after a 52-day FDA review.

K872750 · Lake Medical Products, Inc. · Gastroenterology & Urology device
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Sep 1987
Decision
52d
Days
Class 2
Risk

K872750 is an FDA 510(k) clearance for the LAKE CATHETER CARE KIT. Classified as Catheter, Urological (product code KOD), Class II - Special Controls.

Submitted by Lake Medical Products, Inc. (Maryland Heights, US). The FDA issued a Cleared decision on September 3, 1987 after a review of 52 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5130 - 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 Lake Medical Products, Inc. devices

FDA 510(k) Submission Details - K872750

510(k) Number K872750 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 13, 1987
Decision Date September 03, 1987
Days to Decision 52 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
79d faster than avg
Panel avg: 131d · This submission: 52d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KOD Device Classification - Class 2, Special Controls

Product Code KOD Catheter, Urological
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5130
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 - KOD Catheter, Urological

All 157
Devices cleared under the same product code (KOD) and FDA review panel - the closest regulatory comparables to K872750.
ACKRAD RETROGRADE URETHROGRAPHY SET
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K874517 · American Pharmaseal Div. Ahsc · Dec 1987
ANTIMICROBIAL FOLEY CATHETER
K871429 · American Pharmaseal Div. Ahsc · Aug 1987
KADIR HI-TORQUE GUIDE WIRE
K871297 · Argon Medical Corp. · Apr 1987
PHARMASEAL T TYPE THERMOCOUPLE 100% CATH./PROBE
K870977 · American Pharmaseal Div. Ahsc · Apr 1987