THORTON TITANIUM HOOK ANGLED RIGHT— 510(k) K863988

Name: FDA 510(k) clearance K863988
Creator: U.S. Food and Drug Administration
Published: 1986-10-31

Substantially Equivalent

Keeler Instruments, Inc.

FDA 510(k) clearance K863988 for THORTON TITANIUM HOOK ANGLED RIGHT, Substantially Equivalent on 1986-10-31. Applicant: Keeler Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Keeler Instruments, Inc.
Product code: Code HNQ
Device class: Class 1
Regulation: 21 CFR 886.4350
Advisory panel: Ophthalmic
Date received: 1986-10-14
Decision date: 1986-10-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Broomall, PA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HNQ

view all

K030471 — OPHTEC ENCLAVATION NEEDLE2003-04-17
K022842 — STEPHENS DISPOSABLE HOOKS2002-11-01
K874991 — PRISMA DISPOSABLE IRRIGATING IRIS HOOK1988-04-13
K870440 — LOOK LENS LOOPS1987-02-20
K864292 — DISPOSAL SURGICAL INSTRUMENTS FOR OPHTHALMOLOGY1986-12-29

More clearances from Keeler Instruments, Inc.

view all

K181143 — Keeler TonoCare Tonometer2019-02-08
K112093 — CRYOMATIC CRYO CONSOLE, DISPOSABLE CRYO PROBE, DISPOSABLE PROBE ADAPTER2011-12-08
K093298 — PULSAIR INTELLIPUFF, PULSAIR DESKTOP MODEL 2414-P-2001, 2417-P-20002010-12-10
K100500 — PSL CLASSIC SLIT LAMP2010-03-09
K062412 — CRYOMATIC2006-11-06

Data sourced from openFDA. This site is unofficial and independent of the FDA.