GENERATED RETINAL REFLEX IMAGERY SYS— 510(k) K840840

Name: FDA 510(k) clearance K840840
Creator: U.S. Food and Drug Administration
Published: 1984-07-12

Substantially Equivalent

Electro Optical Instruments

FDA 510(k) clearance K840840 for GENERATED RETINAL REFLEX IMAGERY SYS, Substantially Equivalent on 1984-07-12. Applicant: Electro Optical Instruments. Device class: 1.

Clearance details

Applicant: Electro Optical Instruments
Product code: Code HKM
Device class: Class 1
Regulation: 21 CFR 886.1780
Advisory panel: Ophthalmic
Date received: 1984-02-24
Decision date: 1984-07-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Recent devices under product code HKM

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K964338 — RI-TINISCOPE-SLIT/RI-TINISCOPE SPOT/RI-VISION-SLIT/RI-VISION-SPOT1997-01-09
K950791 — STREAK RETINOSCOPE RX-31995-03-28
K950792 — STREAK RETINOSCOPE RX-3A1995-03-28
K950793 — SPOT RETINOSCOPE RX-3SP1995-03-28
K950794 — STREAK RETINOSCOPE RX-RC1995-03-28

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