CATS®-D Tonometer Prism

FDA 510(k) K203850 · Cats Tonometer, LLC

Substantially Equivalent

510(k) numberK203850

Submission

Device name
CATS®-D Tonometer Prism
Applicant
Cats Tonometer, LLC
Tucson, AZ, US
Received
December 31, 2020
Decision date
June 14, 2021
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HKY – Tonometer, Manual
Device class
Class II (moderate risk)
Regulation
21 CFR 886.1930
Specialty
Ophthalmic

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K234037CATS-L Tonometer™ PrismHKY · Special Cats Tonometer, LLC02/09/2024SE
K232143Applanation Tonometer HT-5000HKY · Traditional Huvitz Co., Ltd.10/23/2023SE
K220852iCare IC200HKY · Traditional Icare Finland OY10/06/2022SE
K211355iCare HOME2HKY · Traditional Icare Finland OY01/25/2022SE
K200966Icare HOME TonometerHKY · Special Icare Finland OY05/07/2020SE
K190316Icare ic200HKY · Traditional Icare Finland OY01/14/2020SE
K191314Sunkingdom Applanation Tonometer SK-R, SK-T, SK-QHKY · Traditional Chongqing Sunkingdom Medical Instrument Co., Ltd.12/19/2019SE
K182491Applanation tonometer AT-2HKY · Traditional Takagi Seiko Co., Ltd.12/10/2018SE

More from Takagi Seiko Co., Ltd.

510(k)DeviceDecision
K234037CATS-L Tonometer™ PrismHKY · Special 02/09/2024SE
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Questions and answers

When was CATS®-D Tonometer Prism cleared by the FDA?

CATS®-D Tonometer Prism (K203850) received a 510(k) decision of Substantially Equivalent on June 14, 2021, 165 days after the submission was received.

What is the product code of K203850?

The FDA product code is HKY – Tonometer, Manual, a Class II (moderate risk) device regulated under 21 CFR 886.1930.