Cleared Abbreviated

K000039 - INVIGRA MALE LATEX CONDOM YELLOW COLORED AND BANANA FLAVORED

K000039 is an FDA 510(k) clearance for INVIGRA MALE LATEX CONDOM YELLOW COLORE..., manufactured by Indus Medicare , Ltd.. The device is a Class 2 Obstetrics & Gynecology device with product code HIS cleared through the Abbreviated 510(k) pathway after a 75-day FDA review.

K000039 · Indus Medicare , Ltd. · Obstetrics & Gynecology device
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Optimized for regulatory review, auditing and printing
Mar 2000
Decision
75d
Days
Class 2
Risk

K000039 is an FDA 510(k) clearance for the INVIGRA MALE LATEX CONDOM YELLOW COLORED AND BANANA FLAVORED. Classified as Condom (product code HIS), Class II - Special Controls.

Submitted by Indus Medicare , Ltd. (Hyderabad Andhra Pradesh, IN). The FDA issued a Cleared decision on March 21, 2000 after a review of 75 days - a notably fast clearance cycle.

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.

View all Indus Medicare , Ltd. devices

FDA 510(k) Submission Details - K000039

510(k) Number K000039 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 06, 2000
Decision Date March 21, 2000
Days to Decision 75 days
Submission Type Abbreviated
Review Panel Obstetrics & Gynecology (OB)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
85d faster than avg
Panel avg: 160d · This submission: 75d
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 134
Devices cleared under the same product code (HIS) and FDA review panel - the closest regulatory comparables to K000039.
REMED MALE TUTTI FRUTTI CONDOM (COCONUT) PREVENTOR, LUCKY BOY, SUMMIT
K993409 · Remed Pharma · Aug 2000
TROJAN EXTRA LARGE LATEX CONDOM
K001212 · Armkel, LLC · May 2000
TROJAN LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT
K000748 · Armkel, LLC · Apr 2000
LOVE LOCKERS
K993733 · Medtech Products , Ltd. · Mar 2000
DOUBLE SPRINGERS
K993735 · Medtech Products , Ltd. · Mar 2000
MIGHTY MAN (DYNAMIC LINKERS)
K993737 · Medtech Products , Ltd. · Mar 2000