ULTRA-WIDE SAFETY SPECTACLE FRAME— 510(k) K813156

Name: FDA 510(k) clearance K813156
Creator: U.S. Food and Drug Administration
Published: 1981-12-14

Substantially Equivalent

Zee Medical Products Co., Inc.

FDA 510(k) clearance K813156 for ULTRA-WIDE SAFETY SPECTACLE FRAME, Substantially Equivalent on 1981-12-14. Applicant: Zee Medical Products Co., Inc.. Device class: 1.

Clearance details

Applicant: Zee Medical Products Co., Inc.
Product code: Code HQZ
Device class: Class 1
Regulation: 21 CFR 886.5842
Advisory panel: Ophthalmic
Date received: 1981-11-06
Decision date: 1981-12-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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 Zee Medical Products Co., Inc.

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K823501 — ZEE SPHYGMOMANOMETER1983-01-21
K813016 — ZEE TRACTION SPLINT1981-11-24
K812814 — ZEE SURGICAL INSTRUMENTS1981-11-06
K812564 — ZEE LIFE SUPPORT AIR PANTS1981-10-23
K812342 — ZEE EXTRICATION DEVICE1981-09-21

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