Cleared Traditional

K052824 - KIMBERLY-CLARK PROCEDURE GOWN

K052824 is an FDA 510(k) clearance for KIMBERLY-CLARK PROCEDURE GOWN, manufactured by Kimberly-Clark Corp.. The device is a Class 2 General Hospital device with product code FYA cleared through the Traditional 510(k) pathway after a 209-day FDA review.

K052824 · Kimberly-Clark Corp. · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 2006
Decision
209d
Days
Class 2
Risk

K052824 is an FDA 510(k) clearance for the KIMBERLY-CLARK PROCEDURE GOWN. Classified as Gown, Surgical (product code FYA), Class II - Special Controls.

Submitted by Kimberly-Clark Corp. (Roswell, US). The FDA issued a Cleared decision on May 2, 2006 after a review of 209 days - an extended review cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 878.4040 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

View all Kimberly-Clark Corp. devices

FDA 510(k) Submission Details - K052824

510(k) Number K052824 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 05, 2005
Decision Date May 02, 2006
Days to Decision 209 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
80d slower than avg
Panel avg: 129d · This submission: 209d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FYA Device Classification - Class 2, Special Controls

Product Code FYA Gown, Surgical
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4040
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 - FYA Gown, Surgical

All 159
Devices cleared under the same product code (FYA) and FDA review panel - the closest regulatory comparables to K052824.
STRYKER T6 HOODS AND TOGAS
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K062899 · Microtek Medical, Inc. · Jan 2007
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K062969 · Medline Industries, Inc. · Dec 2006
COMPE1 1 -PLY SURGICAL GOWNS
K060181 · Standard Textile Co., Inc. · Mar 2006
COMPEL 1-PLY SURGICAL GOWNS
K041653 · Standard Textile Co., Inc. · Jul 2005
COMBOSAFE (EUROPE) AND PROMAX (US) SURGICAL GOWNS
K041540 · Standard Textile Co., Inc. · May 2005