Cleared Traditional

K884925 - THE GREAT WALL CONDOM

K884925 is an FDA 510(k) clearance for THE GREAT WALL CONDOM, manufactured by Pacific Sales & Development Corp.. The device is a Class 2 Obstetrics & Gynecology device with product code HIS cleared through the Traditional 510(k) pathway after a 207-day FDA review.

K884925 · Pacific Sales & Development Corp. · Obstetrics & Gynecology device
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Jun 1989
Decision
207d
Days
Class 2
Risk

K884925 is an FDA 510(k) clearance for the THE GREAT WALL CONDOM. Classified as Condom (product code HIS), Class II - Special Controls.

Submitted by Pacific Sales & Development Corp. (Sonoma, US). The FDA issued a Cleared decision on June 23, 1989 after a review of 207 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 Pacific Sales & Development Corp. devices

FDA 510(k) Submission Details - K884925

510(k) Number K884925 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 28, 1988
Decision Date June 23, 1989
Days to Decision 207 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
47d slower than avg
Panel avg: 160d · This submission: 207d
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 202
Devices cleared under the same product code (HIS) and FDA review panel - the closest regulatory comparables to K884925.
NUDA (CURRENTLY CALLED ULTRA SENSITIVE)
K901111 · Ansell, Inc. · Mar 1990
G.S.A. COLORED CONDOMS
K901112 · Ansell, Inc. · Mar 1990
MAGNUM PLUS LATEX CONDOM W/SPERMICIDAL LUBRICANT
K895640 · Armkel, LLC · Jan 1990
HSV-CHECK(TM) TEST KIT
K890819 · Diagnostic Technology, Inc. · Jun 1989
TROJAN FOR WOMEN
K890863 · Armkel, LLC · Apr 1989
TROJAN EXTRA STRENGTH LUBRICATED
K883413 · Carter Products · Dec 1988