OPHTHALMIC PROJECTOR— 510(k) K921214

Substantially Equivalent

Luneau Ophtalmologie SA

FDA 510(k) clearance K921214 for OPHTHALMIC PROJECTOR, Substantially Equivalent on 1992-06-11. Applicant: Luneau Ophtalmologie SA. Device class: 1.

Clearance details

Applicant: Luneau Ophtalmologie SA
Product code: Code HOS
Device class: Class 1
Regulation: 21 CFR 886.1680
Advisory panel: Ophthalmic
Date received: 1992-03-13
Decision date: 1992-06-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chartres Cedex, FR

Download summary PDF View on FDA.gov ↗

Recent devices under product code HOS

K936200 — WIRELESS CHART PROJECTOR,HCP-W 7211994-09-28
K930443 — MARCO CP-600 AUTO CHART PROJECTOR/CP-1 CHART PROJE1993-07-06
K924784 — BURTON PROJECTOR HEAD - MODEL 6000-H1993-04-05
K890992 — WOODLYN OPHTHALMIC PROJECTOR1989-05-17
K862519 — BAUSCH & LOMB ACCU-CHART 3 ACUITY PROJECTOR1986-07-23

More clearances from Luneau Ophtalmologie SA

K922253 — KERATOREF L601992-06-19
K913961 — OPHTHALMIC STAND1991-12-04

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