Cleared Traditional

STERILIZATION WRAP-STERISHEET (K931202) - FDA 510(k) Clearance

Class II General Hospital device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K931202 · Arjo Wiggins Medical, Inc. · General Hospital
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Dec 1993
Decision
282d
Days
Class 2
Risk

K931202 is an FDA 510(k) clearance for the STERILIZATION WRAP-STERISHEET. Classified as Wrap, Sterilization (product code FRG), Class II - Special Controls.

Submitted by Arjo Wiggins Medical, Inc. (Palm Harbor, US). The FDA issued a Cleared decision on December 16, 1993 after a review of 282 days - an extended review cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6850 - 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 Arjo Wiggins Medical, Inc. devices

Submission Details

510(k) Number K931202 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 09, 1993
Decision Date December 16, 1993
Days to Decision 282 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
153d slower than avg
Panel avg: 129d · This submission: 282d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code FRG Wrap, Sterilization
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.6850
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 - FRG Wrap, Sterilization

All 321
Devices cleared under the same product code (FRG) and FDA review panel - the closest regulatory comparables to K931202.
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K250306 · Propper Manufacturing Co., Inc. · Oct 2025
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K243179 · Yichang Xinxin Paper Products Co., Ltd. · Jun 2025