Home / 510(k) Clearances / K894162

510(k) K894162

OPTISOL by Chiron Ophthalmics — Product Code LYX

K894162 is an FDA 510(k) premarket notification submitted by Chiron Ophthalmics for the device "OPTISOL". The FDA issued a decision of Substantially Equivalent on January 12, 1990. The device falls under product code LYX (Media, Corneal Storage), a Class U device. Chiron Ophthalmics has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 12, 1990
Date Received
June 14, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Media, Corneal Storage
Device Class
Class U
Regulation Number
Review Panel
OP
Submission Type

Other clearances by Chiron Ophthalmics

  • K915861 — MEDILENS-CS CORNEAL SHIELD (March 6, 1992)
  • K914311 — CHIROFLEX II LENS MICROSERT(TM) (January 27, 1992)
  • K905825 — COLLAGEN SHIELD, VARIOUS MODELS (June 10, 1991)
  • K903575 — CHIROFLEX FORCEPS (December 21, 1990)
  • K903574 — CHIROFLEX LENS MICROSERT (September 17, 1990)
  • K901880 — MEDILENS(TM) CORNEAL SHIELD (July 2, 1990)
  • K885015 — COI 72 HR COLLAGEN SHIELD (June 23, 1989)
  • K885016 — COI 24 HR COLLAGEN SHIELD (February 1, 1989)
  • K882762 — COLLAGEN SHIELD (September 12, 1988)

Other clearances for product code LYX

  • K251320 — XTRA4 (September 11, 2025)
  • K221759 — Cornisol (October 5, 2022)
  • K211786 — Independent Corneal Viewing Chamber (IVC-21) (December 3, 2021)
  • K162013 — Eusol-C (September 15, 2016)
  • K151061 — Cornea Cold (August 6, 2015)
  • K063304 — LIFE4C (December 21, 2007)
  • K063617 — EUSOL-C (February 8, 2007)
  • K032422 — EUSOL-C (December 15, 2003)
  • K954548 — THE CHEN MEDIUM (May 20, 1996)
  • K924165 — OPTISOL-GS CORNEAL STORAGE MEDIA (October 6, 1992)

FDA data resources