OPTICAL ZONE/HEXAGONAL/ASTIGMATISM/RADIAL MARKERS— 510(k) K925606

Name: FDA 510(k) clearance K925606
Creator: U.S. Food and Drug Administration
Published: 1994-08-29

Substantially Equivalent

Chiron Vision Corp.

FDA 510(k) clearance K925606 for OPTICAL ZONE/HEXAGONAL/ASTIGMATISM/RADIAL MARKERS, Substantially Equivalent on 1994-08-29. Applicant: Chiron Vision Corp.. Device class: 1.

Clearance details

Applicant: Chiron Vision Corp.
Product code: Code HMR
Device class: Class 1
Regulation: 21 CFR 886.4570
Advisory panel: Ophthalmic
Date received: 1992-11-05
Decision date: 1994-08-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HMR

view all

K053475 — OPTIPOINT CORNEAL MARKER, MODEL VPT-OPT-4502006-03-03
K872747 — LASER CENTERING DEVICE1987-09-04
K863663 — OPHTHALMIC SURGICAL OCULAR MARKERS1986-10-20
K861535 — OPTICAL MARKERS/FIXATION RING/CANNU & IRRIGA CANNU1986-05-14

More clearances from Chiron Vision Corp.

view all

K970727 — MPORT FOLDABLE LENS PLACEMENT SYSTEM1997-12-17
K972808 — HANSATOME MICROKERATOME1997-10-24
K960414 — SYNERGIST POWER PACK1996-04-24
K944993 — IOLAB.SITE CD PHACOEMULSIFICATION MODULE1995-10-12
K944995 — IOLAB/SITE PERISTALTIC MODULE1995-10-05

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