Cleared Traditional

K781780 - CATHETER

K781780 is the FDA 510(k) clearance for CATHETER by Medi-Tech, Inc.. It is a Class 2 Gastroenterology & Urology device (product code KNX) cleared through the Traditional 510(k) pathway after a 50-day FDA review.

K781780 · Medi-Tech, Inc. · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Dec 1978
Decision
50d
Days
Class 2
Risk

K781780 is an FDA 510(k) clearance for the CATHETER, EXTERNAL MALE NURSING CARE. Classified as Collector, Urine, (and Accessories) For Indwelling Catheter (product code KNX), Class II - Special Controls.

Submitted by Medi-Tech, Inc. (Mchenry, US). The FDA issued a Cleared decision on December 7, 1978 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 876.5250 - 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 Medi-Tech, Inc. devices

Submission Details

510(k) Number K781780 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 18, 1978
Decision Date December 07, 1978
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
80d faster than avg
Panel avg: 130d · This submission: 50d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KNX Collector, Urine, (and Accessories) For Indwelling Catheter
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5250
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 - KNX Collector, Urine, (and Accessories) For Indwelling Catheter

All 43
Devices cleared under the same product code (KNX) and FDA review panel - the closest regulatory comparables to K781780.
CONPHAR LEG BAG
K791270 · Conphar, Inc. · Aug 1979
ARGYLE URINE METER
K790969 · Sherwood Medical Co. · Jun 1979
BK-6021 CONDOM CATHETER HOLDER
K790174 · Fred Sammons, Inc. · Feb 1979
LEG BAG
K780878 · Abco Dealers, Inc. · Jul 1978
BAG, URINARY, DRAINAGE, 2D9013
K770762 · Travenol Laboratories, S.A. · May 1977
MEMBRANE SOURCE-EX SERIES DIALYZER CART.
K770516 · Extracorporeal Medical Specialities, Inc. · Mar 1977