VISTA SPECIALIST OPHTHALMOSCOPE (BATTERY & AC)— 510(k) K893173

Name: FDA 510(k) clearance K893173
Creator: U.S. Food and Drug Administration
Published: 1989-06-05

Substantially Equivalent

Keeler Instruments, Inc.

FDA 510(k) clearance K893173 for VISTA SPECIALIST OPHTHALMOSCOPE (BATTERY & AC), Substantially Equivalent on 1989-06-05. Applicant: Keeler Instruments, Inc.. Device class: 2.

Clearance details

Applicant: Keeler Instruments, Inc.
Product code: Code HLI
Device class: Class 2
Regulation: 21 CFR 886.1570
Advisory panel: Ophthalmic
Date received: 1989-04-25
Decision date: 1989-06-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Broomall, PA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HLI

view all

K153080 — RTVue XR OCT Avanti with AngioVue Software2016-02-11
K150722 — EnFocus 2300, EnFocus 44002015-12-02
K142953 — OCT-Camera2015-03-04
K141638 — PROPPER INSIGHT BINOCULAR INDIRECT OPHTHALMOSOPE2014-09-17
K133758 — CENTERVUE MACULAR INTEGRITY ASSESSMENT2014-04-23

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.