Cleared Special

K013025 - MODIFICATION TO FLOUROLAB PLUS

K013025 is an FDA 510(k) clearance for MODIFICATION TO FLOUROLAB PLUS, manufactured by Z-Kat, Inc.. The device is a Class 2 Neurology device with product code HAW cleared through the Special 510(k) pathway after a 23-day FDA review.

K013025 · Z-Kat, Inc. · Neurology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 2001
Decision
23d
Days
Class 2
Risk

K013025 is an FDA 510(k) clearance for the MODIFICATION TO FLOUROLAB PLUS. Classified as Neurological Stereotaxic Instrument (product code HAW), Class II - Special Controls.

Submitted by Z-Kat, Inc. (Hollywood, US). The FDA issued a Cleared decision on October 3, 2001 after a review of 23 days - a notably fast clearance cycle.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.4560 - the FDA neurology device framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Z-Kat, Inc. devices

FDA 510(k) Submission Details - K013025

510(k) Number K013025 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 10, 2001
Decision Date October 03, 2001
Days to Decision 23 days
Submission Type Special
Review Panel Neurology (NE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
125d faster than avg
Panel avg: 148d · This submission: 23d
Pathway characteristics
Modification to existing cleared device.

HAW Device Classification - Class 2, Special Controls

Product Code HAW Neurological Stereotaxic Instrument
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.4560
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 Neurology devices follow this clearance model.

Regulatory Peers - HAW Neurological Stereotaxic Instrument

All 287
Devices cleared under the same product code (HAW) and FDA review panel - the closest regulatory comparables to K013025.
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