OPHTHALMIC TRIAL LENSES— 510(k) K930195

Name: FDA 510(k) clearance K930195
Creator: U.S. Food and Drug Administration
Published: 1994-01-06

Substantially Equivalent

Optimark Accessories and Instruments

FDA 510(k) clearance K930195 for OPHTHALMIC TRIAL LENSES, Substantially Equivalent on 1994-01-06. Applicant: Optimark Accessories and Instruments. Device class: 1.

Clearance details

Applicant: Optimark Accessories and Instruments
Product code: Code HPC
Device class: Class 1
Regulation: 21 CFR 886.1405
Advisory panel: Ophthalmic
Date received: 1993-01-14
Decision date: 1994-01-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seattle, WA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HPC

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K945443 — BOBES LENS SET1995-07-19
K951437 — OTI MODEL TLS-601995-04-11
K934859 — CONTACT LENSES1993-12-21
K930446 — MARCO TRIAL SETS1993-07-06
K924786 — BURTON TRIAL LENS SET1993-04-14

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