Cleared Abbreviated

K992081 - VARIOUS ANSELL TRADENAMES OR PRIVATE LABEL

K992081 is an FDA 510(k) clearance for VARIOUS ANSELL TRADENAMES OR PRIVATE LABEL, manufactured by Suretex Prophylactics (India) , Ltd.. The device is a Class 2 Obstetrics & Gynecology device with product code HIS cleared through the Abbreviated 510(k) pathway after a 59-day FDA review.

K992081 · Suretex Prophylactics (India) , Ltd. · Obstetrics & Gynecology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 1999
Decision
59d
Days
Class 2
Risk

K992081 is an FDA 510(k) clearance for the VARIOUS ANSELL TRADENAMES OR PRIVATE LABEL. Classified as Condom (product code HIS), Class II - Special Controls.

Submitted by Suretex Prophylactics (India) , Ltd. (Dothan, US). The FDA issued a Cleared decision on August 19, 1999 after a review of 59 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 Suretex Prophylactics (India) , Ltd. devices

FDA 510(k) Submission Details - K992081

510(k) Number K992081 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 21, 1999
Decision Date August 19, 1999
Days to Decision 59 days
Submission Type Abbreviated
Review Panel Obstetrics & Gynecology (OB)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
101d faster than avg
Panel avg: 160d · This submission: 59d
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 110
Devices cleared under the same product code (HIS) and FDA review panel - the closest regulatory comparables to K992081.
TROJAN MINT TINGLE BRAND LATEX CONDOMS
K023405 · Armkel, LLC · Dec 2002
TROJAN EXTRA LARGE LATEX CONDOM
K001212 · Armkel, LLC · May 2000
TROJAN LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT
K000748 · Armkel, LLC · Apr 2000
ANSELL CONDOMS
K984392 · Ansell, Inc. · Jul 1999
LIFESTYLES XTRA PLEASURE
K983518 · Ansell, Inc. · Jul 1999
CVS PERSONAL LUBRICANT
K983216 · San-Mar Laboratories, Inc. · May 1999