Cleared Traditional

K091890 - EXTENDED USE ALDAHOL HIGH LEVEL DISINFE...

K091890 is an FDA 510(k) clearance for EXTENDED USE ALDAHOL HIGH LEVEL DISINFE..., manufactured by Healthpoint, Ltd.. The device is a Class 2 General Hospital device with product code MED cleared through the Traditional 510(k) pathway after a 274-day FDA review.

K091890 · Healthpoint, Ltd. · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 2010
Decision
274d
Days
Class 2
Risk

K091890 is an FDA 510(k) clearance for the EXTENDED USE ALDAHOL HIGH LEVEL DISINFECTANT. Classified as Sterilant, Medical Devices (product code MED), Class II - Special Controls.

Submitted by Healthpoint, Ltd. (Fort Worth, US). The FDA issued a Cleared decision on March 24, 2010 after a review of 274 days - an extended review cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6885 - 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 Healthpoint, Ltd. devices

FDA 510(k) Submission Details - K091890

510(k) Number K091890 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 23, 2009
Decision Date March 24, 2010
Days to Decision 274 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
145d slower than avg
Panel avg: 129d · This submission: 274d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MED Device Classification - Class 2, Special Controls

Product Code MED Sterilant, Medical Devices
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.6885
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 - MED Sterilant, Medical Devices

All 31
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