Cleared Traditional

K020393 - MASTER & FRANK SURGICAL DRAPES (STERILE)

K020393 is an FDA 510(k) clearance for MASTER & FRANK SURGICAL DRAPES (STERILE), manufactured by Master & Frank Enterprses Co., Ltd.. The device is a Class 2 General Hospital device with product code KKX cleared through the Traditional 510(k) pathway after a 86-day FDA review.

K020393 · Master & Frank Enterprses Co., Ltd. · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 2002
Decision
86d
Days
Class 2
Risk

K020393 is an FDA 510(k) clearance for the MASTER & FRANK SURGICAL DRAPES (STERILE). Classified as Drape, Surgical (product code KKX), Class II - Special Controls.

Submitted by Master & Frank Enterprses Co., Ltd. (Taipei, TW). The FDA issued a Cleared decision on May 3, 2002 after a review of 86 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 878.4370 - the FDA general hospital 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 Master & Frank Enterprses Co., Ltd. devices

FDA 510(k) Submission Details - K020393

510(k) Number K020393 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 06, 2002
Decision Date May 03, 2002
Days to Decision 86 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
43d faster than avg
Panel avg: 129d · This submission: 86d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KKX Device Classification - Class 2, Special Controls

Product Code KKX Drape, Surgical
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4370
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 General Hospital devices follow this clearance model.

Regulatory Peers - KKX Drape, Surgical

All 250
Devices cleared under the same product code (KKX) and FDA review panel - the closest regulatory comparables to K020393.
TRILAMINATE DRAPES/TIBURON
K023419 · Allegiance Healthcare Corp. · Feb 2003
DRAPES WITH ABSORBENT REINFORCEMENT
K023425 · Allegiance Healthcare Corp. · Nov 2002
MEDLINE ASEP PLUS SURGICAL DRAPES
K023432 · Medline Industries, Inc. · Nov 2002
WOUND PROTECTOR/RETRACTOR
K020435 · Applied Medical Resources Corp. · Apr 2002
TOWEL DRAPE, MODELS 4409, 4410
K012957 · Dynarex Corp. · Mar 2002
MODIFICATION TO: COMPEL SURGICAL DRAPES
K012807 · Standard Textile Co., Inc. · Oct 2001