SEIKO EYEGLASS FRAME— 510(k) K942513

Name: FDA 510(k) clearance K942513
Creator: U.S. Food and Drug Administration
Published: 1994-07-15

Substantially Equivalent

Seiko Optical Products of America, Inc.

FDA 510(k) clearance K942513 for SEIKO EYEGLASS FRAME, Substantially Equivalent on 1994-07-15. Applicant: Seiko Optical Products of America, Inc.. Device class: 1.

Clearance details

Applicant: Seiko Optical Products of America, Inc.
Product code: Code HQZ
Device class: Class 1
Regulation: 21 CFR 886.5842
Advisory panel: Ophthalmic
Date received: 1994-05-26
Decision date: 1994-07-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mahwah, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HQZ

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K952597 — VIEW POINT, DORION, RUDDY PROJECT, ULTRA FLEX, TRILLON, BAY BOY, SHIELD SKI, SUN POCKETS, POINT OF VIEW1995-09-12
K944313 — SPECTACLE FRAME1995-03-28
K945176 — SPECTACLE FRAME OR EYEGLASS FRAMES1994-12-15
K945392 — SPECTACLE FRAME1994-12-15
K945770 — OPTICAL FRAMES1994-12-15

More clearances from Seiko Optical Products of America, Inc.

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K900764 — SUNGLASS, NON-PRESCRIPTION1990-06-20
K873245 — AR DIACOAT SINGLE VISION LENSES1987-10-05
K861684 — SEIKO P-2 & SEIKO P-3 (SPECTACLE LENS)1986-06-09

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