Cleared Traditional

K970581 - CLINIJEL

K970581 is an FDA 510(k) clearance for CLINIJEL, manufactured by Hospicon Products. The device is a Class 2 Obstetrics & Gynecology device with product code HIS cleared through the Traditional 510(k) pathway after a 201-day FDA review.

K970581 · Hospicon Products · Obstetrics & Gynecology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 1997
Decision
201d
Days
Class 2
Risk

K970581 is an FDA 510(k) clearance for the CLINIJEL. Classified as Condom (product code HIS), Class II - Special Controls.

Submitted by Hospicon Products (London, GB). The FDA issued a Cleared decision on September 3, 1997 after a review of 201 days - an extended review 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 Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Obstetrics & Gynecology review framework, consistent with the majority of Class II 510(k) submissions.

View all Hospicon Products devices

FDA 510(k) Submission Details - K970581

510(k) Number K970581 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 14, 1997
Decision Date September 03, 1997
Days to Decision 201 days
Submission Type Traditional
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
41d slower than avg
Panel avg: 160d · This submission: 201d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

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 96
Devices cleared under the same product code (HIS) and FDA review panel - the closest regulatory comparables to K970581.
LATEX CONDOMS NATURAL COLOUR WITH SILICONE OIL LUBRICANT
K974323 · Reddy Medtech Health Products , Ltd. · Feb 1998
PERSONAL LUBRICATING LIQUID
K973780 · Qualis, Inc. · Nov 1997
VERY PRIVATE INTIMATE MOISTURE
K971793 · Brandwynne Corp. · Nov 1997
ROYALE BRAND LATEX CONDOMS (SILICONE)-COLORED/ASSORTED COLORS
K971132 · G. Premjee (Usa), Inc. · Sep 1997
EXTRAWEAR, GENTLEMEN'S CHOICE
K972428 · Custom Services Intl., Inc. · Aug 1997
INNERWEAR, JIMMY-O RAINCOAT, RAINCOAT, JASMINE, DRINK
K972427 · Custom Services Intl., Inc. · Aug 1997