Portable Non-Contact Tonometer, Model PT100

FDA 510(k) K013259 · Leica Microsystems, Inc. O.I.D.

Substantially Equivalent

510(k) numberK013259

Submission

Device name
Portable Non-Contact Tonometer, Model PT100
Applicant
Leica Microsystems, Inc. O.I.D.
Depew, NY, US
Received
October 1, 2001
Decision date
February 20, 2002
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
HKX – Tonometer, Ac-Powered
Device class
Class II (moderate risk)
Regulation
21 CFR 886.1930
Specialty
Ophthalmic

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Questions and answers

When was Portable Non-Contact Tonometer, Model PT100 cleared by the FDA?

Portable Non-Contact Tonometer, Model PT100 (K013259) received a 510(k) decision of Substantially Equivalent on February 20, 2002, 142 days after the submission was received.

What is the product code of K013259?

The FDA product code is HKX – Tonometer, Ac-Powered, a Class II (moderate risk) device regulated under 21 CFR 886.1930.