CR-39 TYPE RESIN— 510(k) K850905

Substantially Equivalent

Orplex Corp.

FDA 510(k) clearance K850905 for CR-39 TYPE RESIN, Substantially Equivalent on 1985-03-20. Applicant: Orplex Corp.. Device class: 1.

Clearance details

Applicant: Orplex Corp.
Product code: Code HQG
Device class: Class 1
Regulation: 21 CFR 886.5844
Advisory panel: Ophthalmic
Date received: 1985-03-05
Decision date: 1985-03-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HQG

K935919 — SUNGLASSES1994-02-16
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K900091 — MODIFIED OPHTHALMIC OPIR ONUFRYK IMAGE DEFLECTOR1990-04-04
K884360 — SEIKO P-6 PROGRESSIVE SPECTACLE LENSES1988-11-15
K882814 — NEOLENS PRESCRIPTION SPECTACLE LENS1988-07-29

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