ULTRAMATIC PROJECT-O-CHART OPHTH. PROJ— 510(k) K811180

Name: FDA 510(k) clearance K811180
Creator: U.S. Food and Drug Administration
Published: 1981-05-15

Substantially Equivalent

American Optical Corp.

FDA 510(k) clearance K811180 for ULTRAMATIC PROJECT-O-CHART OPHTH. PROJ, Substantially Equivalent on 1981-05-15. Applicant: American Optical Corp.. Device class: 1.

Clearance details

Applicant: American Optical Corp.
Product code: Code HOS
Device class: Class 1
Regulation: 21 CFR 886.1680
Advisory panel: Ophthalmic
Date received: 1981-04-28
Decision date: 1981-05-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HOS

view all

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
K921214 — OPHTHALMIC PROJECTOR1992-06-11
K890992 — WOODLYN OPHTHALMIC PROJECTOR1989-05-17

More clearances from American Optical Corp.

view all

K950881 — PHACO TIP1995-09-06
K950880 — AOI UNIVERSAL ULTRASONIC HANDPIECE1995-05-26
K931354 — P4000 PHACOEMULSIFIER1994-02-22
K931358 — AORP4000 REUSABLE PAK1994-02-22
K931357 — AOD4000 DISPOSABLE PAK1994-01-25

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