Cleared Special

K141750 - HEMOCUE HBA1C 501 GLYCOSYLATED HEMOGLOB...

K141750 is the FDA 510(k) clearance for HEMOCUE HBA1C 501 GLYCOSYLATED HEMOGLOB... by Infopia Co, Ltd.. It is a Class 2 Chemistry device (product code LCP) cleared through the Special 510(k) pathway after a 24-day FDA review.

K141750 · Infopia Co, Ltd. · Chemistry device
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Jul 2014
Decision
24d
Days
Class 2
Risk

K141750 is an FDA 510(k) clearance for the HEMOCUE HBA1C 501 GLYCOSYLATED HEMOGLOBIN MONITORING SYSTEM. Classified as Assay, Glycosylated Hemoglobin (product code LCP), Class II - Special Controls.

Submitted by Infopia Co, Ltd. (Fullerton, US). The FDA issued a Cleared decision on July 24, 2014 after a review of 24 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 864.7470 - the FDA in vitro diagnostics and chemistry 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 Infopia Co, Ltd. devices

Submission Details

510(k) Number K141750 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 30, 2014
Decision Date July 24, 2014
Days to Decision 24 days
Submission Type Special
Review Panel Chemistry (CH)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
64d faster than avg
Panel avg: 88d · This submission: 24d
Pathway characteristics
Modification to existing cleared device.

Device Classification

Product Code LCP Assay, Glycosylated Hemoglobin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 864.7470
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 Chemistry devices follow this clearance model.

Regulatory Peers - LCP Assay, Glycosylated Hemoglobin

All 137
Devices cleared under the same product code (LCP) and FDA review panel - the closest regulatory comparables to K141750.
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K131307 · Siemens Healthcare Diagnostics, Inc. · Jan 2014