Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

OPTO LINE SRL

K-Number: K933809 · 1993-10-18

ApplicantOptoline S.R.L.
Decision Date1993-10-18
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OPTO LINE SRL is the device name listed in this FDA 510(k) record. The listed applicant is Optoline S.R.L.. It received FDA 510(k) clearance on 1993-10-18 under 510(k) number K933809. The device is classified under product code HQZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPTO LINE SRL?

OPTO LINE SRL is a medical device that received FDA 510(k) clearance on 1993-10-18. The listed applicant is Optoline S.R.L.. The 510(k) number is K933809.

When did OPTO LINE SRL receive FDA 510(k) clearance?

OPTO LINE SRL received FDA 510(k) clearance on 1993-10-18, under 510(k) number K933809.

Who is the listed applicant for OPTO LINE SRL?

The FDA 510(k) record lists Optoline S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OPTO LINE SRL?

The FDA product code for OPTO LINE SRL is HQZ.

Related Devices (Code: HQZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K952597VIEW POINT, DORION, RUDDY PROJECT, ULTRA FLEX, TRILLON, BAY BOY, SHIELD SKI, SUN POCKETS, POINT OF VIEWPoint of View Optical Outlet, Inc.K944313SPECTACLE FRAMESun Hing Optical Manufactory , Ltd.K945392SPECTACLE FRAMESeo Han Corp., Ltd.K945176SPECTACLE FRAME OR EYEGLASS FRAMESOptipia Trading Co.K945770OPTICAL FRAMESRamada Optics, Inc.K945350FRAME, SPECTACLESTaiwan Eva Industrial Co., Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑