Thorton Titanium Hook Angled Right

FDA 510(k) K863988 · Keeler Instruments, Inc.

Substantially Equivalent

510(k) numberK863988

Submission

Device name
Thorton Titanium Hook Angled Right
Applicant
Keeler Instruments, Inc.
Broomall, PA, US
Received
October 14, 1986
Decision date
October 31, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
HNQ – Hook, Ophthalmic
Device class
Class I (low risk)
Regulation
21 CFR 886.4350
Specialty
Ophthalmic

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K864292Disposal Surgical Instruments for OphthalmologyHNQ · Traditional Eye-Ko, Inc.12/29/1986SE
K801469Bonn Micro Iris Hook (Non-Sterile) #7613HNQ · Traditional Edward Weck, Inc.07/28/1980SE
K791985Hooks #'S 7600,7602,7603,7616HNQ · Traditional Edward Weck, Inc.10/04/1979SE
K770103Hook, Iris, Shepard U-ShapedHNQ · Traditional Edward Weck, Inc.01/25/1977SE
K770098Hook, Iris, HershmanHNQ · Traditional Edward Weck, Inc.01/24/1977SE

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Questions and answers

When was Thorton Titanium Hook Angled Right cleared by the FDA?

Thorton Titanium Hook Angled Right (K863988) received a 510(k) decision of Substantially Equivalent on October 31, 1986, 17 days after the submission was received.

What is the product code of K863988?

The FDA product code is HNQ – Hook, Ophthalmic, a Class I (low risk) device regulated under 21 CFR 886.4350.