Cleared Traditional

K063873 - ICARE TONOMETER TA01I

K063873 is an FDA 510(k) clearance for ICARE TONOMETER TA01I, manufactured by Tiolat OY. The device is a Class 2 Ophthalmic device with product code HKY cleared through the Traditional 510(k) pathway after a 145-day FDA review.

K063873 · Tiolat OY · Ophthalmic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 2007
Decision
145d
Days
Class 2
Risk

K063873 is an FDA 510(k) clearance for the ICARE TONOMETER TA01I. Classified as Tonometer, Manual (product code HKY), Class II - Special Controls.

Submitted by Tiolat OY (Tampa, US). The FDA issued a Cleared decision on May 23, 2007 after a review of 145 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.

View all Tiolat OY devices

FDA 510(k) Submission Details - K063873

510(k) Number K063873 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 29, 2006
Decision Date May 23, 2007
Days to Decision 145 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
35d slower than avg
Panel avg: 110d · This submission: 145d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HKY Device Classification - Class 2, Special Controls

Product Code HKY Tonometer, Manual
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 - HKY Tonometer, Manual

All 26
Devices cleared under the same product code (HKY) and FDA review panel - the closest regulatory comparables to K063873.
Applanation tonometer AT-2
K182491 · Takagi Seiko Co., Ltd. · Dec 2018
AT 030
K180839 · Carl Zeiss Meditec, AG · Jun 2018
CATS Tonometer Prism
K173904 · Cats Tonometer, LLC · Mar 2018
TONO-PEN AVIA TONOMETER AND OCU-SHILED TIP COVER
K053430 · Medtronic Xomed, Inc. · Mar 2006
PROVIEW EYE PRESSURE MONITOR
K011199 · Bausch & Lomb, Inc. · Jul 2001
C.S.O. TONOMETER
K992835 · Cso · Jun 2000