Cleared Traditional

K020969 - VACURECT VACUUM CONSTRICTION DEVICE

K020969 is an FDA 510(k) clearance for VACURECT VACUUM CONSTRICTION DEVICE, manufactured by Vacurect Manufacturing (Pty) , Ltd.. The device is a Class 2 Gastroenterology & Urology device with product code LKY cleared through the Traditional 510(k) pathway after a 71-day FDA review.

K020969 · Vacurect Manufacturing (Pty) , Ltd. · Gastroenterology & Urology device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Jun 2002
Decision
71d
Days
Class 2
Risk

K020969 is an FDA 510(k) clearance for the VACURECT VACUUM CONSTRICTION DEVICE. Classified as Device, External Penile Rigidity (product code LKY), Class II - Special Controls.

Submitted by Vacurect Manufacturing (Pty) , Ltd. (North Attleboro, US). The FDA issued a Cleared decision on June 5, 2002 after a review of 71 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5020 - the FDA gastroenterology and urology 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Vacurect Manufacturing (Pty) , Ltd. devices

FDA 510(k) Submission Details - K020969

510(k) Number K020969 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 26, 2002
Decision Date June 05, 2002
Days to Decision 71 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
60d faster than avg
Panel avg: 131d · This submission: 71d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LKY Device Classification - Class 2, Special Controls

Product Code LKY Device, External Penile Rigidity
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5020
Definition Intended To Create Or Maintain Sufficient Penile Rigidity For Sexual Intercourse. These Include Vacuum Pumps, Constriction Rings, And Penile Splints, Which Are Mechanical, Powered Or Pneumatic Devices.
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 Gastroenterology & Urology devices follow this clearance model.

Regulatory Peers - LKY Device, External Penile Rigidity

All 61
Devices cleared under the same product code (LKY) and FDA review panel - the closest regulatory comparables to K020969.
NANMA VACUUM PUMP
K030913 · Nanma Mfg Co., Ltd. · Jun 2003
MODIFICATION TO NANMA VACUUM PUMP
K013113 · Nanma Mfg Co., Ltd. · Dec 2002
NANMA ADJUSTABLE CONSTRICTION RING
K013051 · Nanma Mfg Co., Ltd. · Aug 2002
MODIFICATION TO NANMA NON-ADJUSTABLE CONSTRICTION RING
K013053 · Nanma Mfg Co., Ltd. · May 2002
VT-1
K020154 · Pos-T-Vac, Inc. · Apr 2002
SUPPORT SLEEVE
K020258 · Pos-T-Vac, Inc. · Apr 2002