SEIKO P-6 PROGRESSIVE SPECTACLE LENSES— 510(k) K884360

Name: FDA 510(k) clearance K884360
Creator: U.S. Food and Drug Administration
Published: 1988-11-15

Substantially Equivalent

Seiko Corp.

FDA 510(k) clearance K884360 for SEIKO P-6 PROGRESSIVE SPECTACLE LENSES, Substantially Equivalent on 1988-11-15. Applicant: Seiko Corp.. Device class: 1.

Clearance details

Applicant: Seiko Corp.
Product code: Code HQG
Device class: Class 1
Regulation: 21 CFR 886.5844
Advisory panel: Ophthalmic
Date received: 1988-10-17
Decision date: 1988-11-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mahwah, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HQG

view all

K935919 — SUNGLASSES1994-02-16
K920795 — 0R 160, OR-1.60, AND ORCOLITE 1.60 HIGH INDEX1992-07-13
K900091 — MODIFIED OPHTHALMIC OPIR ONUFRYK IMAGE DEFLECTOR1990-04-04
K882814 — NEOLENS PRESCRIPTION SPECTACLE LENS1988-07-29
K882308 — CR-39 PLASTIC LENSES FOR EYEGLASSES1988-07-22

More clearances from Seiko Corp.

view all

K900732 — SPECTACLE FRAME1990-06-20

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