Cleared Traditional

K962176 - TPP

K962176 is the FDA 510(k) clearance for TPP by Panbio, Inc.. It is a Class 2 Hematology device (product code MIF) cleared through the Traditional 510(k) pathway after a 135-day FDA review.

K962176 · Panbio, Inc. · Hematology device
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Oct 1996
Decision
135d
Days
Class 2
Risk

K962176 is an FDA 510(k) clearance for the TPP. Classified as Prothrombin Fragment 1.2 (product code MIF), Class II - Special Controls.

Submitted by Panbio, Inc. (South Bend, US). The FDA issued a Cleared decision on October 18, 1996 after a review of 135 days - within the typical 510(k) review window.

This device falls under the Hematology FDA review panel, regulated under 21 CFR 864.7320 - the FDA hematology 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 Hematology review framework, consistent with the majority of Class II 510(k) submissions.

View all Panbio, Inc. devices

Submission Details

510(k) Number K962176 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 05, 1996
Decision Date October 18, 1996
Days to Decision 135 days
Submission Type Traditional
Review Panel Hematology (HE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
22d slower than avg
Panel avg: 113d · This submission: 135d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code MIF Prothrombin Fragment 1.2
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 864.7320
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 Hematology devices follow this clearance model.

Regulatory Peers - MIF Prothrombin Fragment 1.2

Devices cleared under the same product code (MIF) and FDA review panel - the closest regulatory comparables to K962176.
ENZYGNOST F+2 (MONOCLONAL) TEST KIT
K042687 · Dade Behring, Inc. · Dec 2004
THROMBONOSTIKA F1.2
K964934 · Organon Teknika Corp. · Mar 1997
ENZYGNOST F 1+2
K922934 · Behring Diagnostics, Inc. · Nov 1992
DADE(R) PROTHROMBIN FRAGMENT F1.2 ELISA
K920895 · Baxter Diagnostics, Inc. · Jun 1992
THROMBONOSTIKA F1.2
K911434 · Organon Teknika Corp. · Oct 1991