Cleared Abbreviated

K063401 - BANANA RIBBED

K063401 is an FDA 510(k) clearance for BANANA RIBBED, manufactured by Medtech Products , Ltd.. The device is a Class 2 Obstetrics & Gynecology device with product code HIS cleared through the Abbreviated 510(k) pathway after a 137-day FDA review.

K063401 · Medtech Products , Ltd. · Obstetrics & Gynecology device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Mar 2007
Decision
137d
Days
Class 2
Risk

K063401 is an FDA 510(k) clearance for the BANANA RIBBED. Classified as Condom (product code HIS), Class II - Special Controls.

Submitted by Medtech Products , Ltd. (Bellevue, US). The FDA issued a Cleared decision on March 26, 2007 after a review of 137 days - within the typical 510(k) review window.

This device falls under the Obstetrics & Gynecology FDA review panel, regulated under 21 CFR 884.5300 - the FDA obstetrics and gynecology device framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.

FDA 510(k) Submission Details - K063401

510(k) Number K063401 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 09, 2006
Decision Date March 26, 2007
Days to Decision 137 days
Submission Type Abbreviated
Review Panel Obstetrics & Gynecology (OB)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
24d faster than avg
Panel avg: 161d · This submission: 137d
Pathway characteristics
Standards-based clearance path.

HIS Device Classification - Class 2, Special Controls

Product Code HIS Condom
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 884.5300
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 Obstetrics & Gynecology devices follow this clearance model.

Regulatory Peers - HIS Condom

All 360
Devices cleared under the same product code (HIS) and FDA review panel - the closest regulatory comparables to K063401.
MULTIPLE BRAND MALE LATEX CONDOM
K070937 · Nulatex Sdn. Bhd. · Sep 2007
TROJAN THINTENSITY BRAND MALE LATEX CONDOM
K071272 · Church & Dwight Co., Inc. · Sep 2007
MALE NATURAL RUBBER LATEX CONDOM (WITH COLORING AND FLAVORING)
K070830 · Karex Industries Sdn. Bhd. · May 2007
NON-SPERMICIDAL LUBRICATED MALE LATEX CONDOMS
K062730 · Biogreen Medical Sdn. Bhd. · Oct 2006
ZEUS MALE CONDOM APPLICATOR
K052206 · Condax, LLC · Sep 2006
GREEN LOVE MALE CONTRACEPTIVE (CONDOM)
K051842 · Cupid Condom, Ltd. · Apr 2006
K063401 · BANANA RIBBED
Download PDF FDA Summary Medtech Products , Lt…