Cleared Traditional

K172825 - MN-111

K172825 is an FDA 510(k) clearance for MN-111, manufactured by W&H Sterilization S.R.L.. The device is a Class 2 General Hospital device with product code FLE cleared through the Traditional 510(k) pathway after a 254-day FDA review.

K172825 · W&H Sterilization S.R.L. · General Hospital
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May 2018
Decision
254d
Days
Class 2
Risk

K172825 is an FDA 510(k) clearance for the MN-111. Classified as Sterilizer, Steam (product code FLE), Class II - Special Controls.

Submitted by W&H Sterilization S.R.L. (Brusaporto, IT). The FDA issued a Cleared decision on May 30, 2018 after a review of 254 days - an extended review cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6880 - 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 W&H Sterilization S.R.L. devices

FDA 510(k) Submission Details - K172825

510(k) Number K172825 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 18, 2017
Decision Date May 30, 2018
Days to Decision 254 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
125d slower than avg
Panel avg: 129d · This submission: 254d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FLE Device Classification - Class 2, Special Controls

Product Code FLE Sterilizer, Steam
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.6880
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 - FLE Sterilizer, Steam

All 75
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