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FDA 510(k)

ILO MADE IN ITALY; GARBO HAND FINISHED ITALY

K-Number: K943296 · 1994-09-14

ApplicantIlo Industria Lombarda Ottica Srl
Decision Date1994-09-14
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ILO MADE IN ITALY; GARBO HAND FINISHED ITALY is the device name listed in this FDA 510(k) record. The listed applicant is Ilo Industria Lombarda Ottica Srl. It received FDA 510(k) clearance on 1994-09-14 under 510(k) number K943296. The device is classified under product code HQY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ILO MADE IN ITALY; GARBO HAND FINISHED ITALY?

ILO MADE IN ITALY; GARBO HAND FINISHED ITALY is a medical device that received FDA 510(k) clearance on 1994-09-14. The listed applicant is Ilo Industria Lombarda Ottica Srl. The 510(k) number is K943296.

When did ILO MADE IN ITALY; GARBO HAND FINISHED ITALY receive FDA 510(k) clearance?

ILO MADE IN ITALY; GARBO HAND FINISHED ITALY received FDA 510(k) clearance on 1994-09-14, under 510(k) number K943296.

Who is the listed applicant for ILO MADE IN ITALY; GARBO HAND FINISHED ITALY?

The FDA 510(k) record lists Ilo Industria Lombarda Ottica Srl as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ILO MADE IN ITALY; GARBO HAND FINISHED ITALY?

The FDA product code for ILO MADE IN ITALY; GARBO HAND FINISHED ITALY is HQY.

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Related Devices (Code: HQY)

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Official Source

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

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