Cleared Traditional

K920995 - BARRIER DRAPE SHEET WITH SYMETRY FABRIC

K920995 is the FDA 510(k) clearance for BARRIER DRAPE SHEET WITH SYMETRY FABRIC by Johnson & Johnson Medical, Inc.. It is a Class 2 General Hospital device (product code KKX) cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K920995 · Johnson & Johnson Medical, Inc. · General Hospital
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May 1992
Decision
90d
Days
Class 2
Risk

K920995 is an FDA 510(k) clearance for the BARRIER DRAPE SHEET WITH SYMETRY FABRIC. Classified as Drape, Surgical (product code KKX), Class II - Special Controls.

Submitted by Johnson & Johnson Medical, Inc. (Arlington, US). The FDA issued a Cleared decision on May 31, 1992 after a review of 90 days - within the typical 510(k) review window.

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: 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 Johnson & Johnson Medical, Inc. devices

Submission Details

510(k) Number K920995 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 02, 1992
Decision Date May 31, 1992
Days to Decision 90 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
39d faster than avg
Panel avg: 129d · This submission: 90d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 147
Devices cleared under the same product code (KKX) and FDA review panel - the closest regulatory comparables to K920995.
DELUXE WOUND CLOSURE TRAY, STERILE, DISPOSABLE
K921204 · Trinity Laboratories, Inc. · Aug 1992
DRESSING CHANGE TRAY, STERILE, DISPOSABLE
K921394 · Trinity Laboratories, Inc. · Aug 1992
QUALTEX TUBE/CORD ORGANIZER
K921350 · Deroyal Industries, Inc. · Aug 1992
MINOR LACERATION TRAY W/ INSTRUMENT, STERILE, DISP
K920517 · Trinity Laboratories, Inc. · May 1992
QUALTEX SURGICAL DRAPE, MODIFICATION
K913486 · Deroyal Industries, Inc. · Feb 1992
ARTHROSCOPY CAMERA DRAPE
K915214 · O.R. Concepts, Inc. · Jan 1992