Cleared Traditional

K013259 - PORTABLE NON-CONTACT TONOMETER, MODEL PT100

K013259 is an FDA 510(k) clearance for PORTABLE NON-CONTACT TONOMETER, manufactured by Leica Microsystems, Inc. O.I.D.. The device is a Class 2 Ophthalmic device with product code HKX cleared through the Traditional 510(k) pathway after a 142-day FDA review.

K013259 · Leica Microsystems, Inc. O.I.D. · Ophthalmic device
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Feb 2002
Decision
142d
Days
Class 2
Risk

K013259 is an FDA 510(k) clearance for the PORTABLE NON-CONTACT TONOMETER, MODEL PT100. Classified as Tonometer, Ac-powered (product code HKX), Class II - Special Controls.

Submitted by Leica Microsystems, Inc. O.I.D. (Depew, US). The FDA issued a Cleared decision on February 20, 2002 after a review of 142 days - within the typical 510(k) review window.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.1930 - the FDA ophthalmic 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 Ophthalmic review framework, consistent with the majority of Class II 510(k) submissions.

FDA 510(k) Submission Details - K013259

510(k) Number K013259 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 01, 2001
Decision Date February 20, 2002
Days to Decision 142 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
32d slower than avg
Panel avg: 110d · This submission: 142d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HKX Device Classification - Class 2, Special Controls

Product Code HKX Tonometer, Ac-powered
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 886.1930
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 Ophthalmic devices follow this clearance model.

Regulatory Peers - HKX Tonometer, Ac-powered

All 57
Devices cleared under the same product code (HKX) and FDA review panel - the closest regulatory comparables to K013259.
CANON FULL AUTO TONOMETER TX-F
K023816 · Canon, Inc.-Utsunomiya Optical Products Operation · Nov 2002
KOWA AUTOMATED TONOMETER KT-500
K013805 · Kowa Optimed, Inc. · Oct 2002
TGDC-01 PRA
K021937 · Truevision Instruments · Oct 2002
LANGHAM OCULAR BLOOD FLOW (OBF) TONOGRAPH/TONOMETER MODEL 201
K010998 · Langham Ophthalmic Technologies · Jun 2001
MODEL 30 CLASSIC PNEUMATONOMETER
K002395 · Xomed, Inc. · Dec 2000
SMARTLENS
K002510 · Odc Ophthalmic Development Co. AG · Oct 2000
K013259 · PORTABLE NON-CONTACT TONOMETER, MODEL PT100
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