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FDA 510(k)

APEX OPTICAL IND. CO., EYE WEA MODELS

K-Number: K932821 · 1994-01-25

ApplicantApex Optical Ind. Co.
Decision Date1994-01-25
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

APEX OPTICAL IND. CO., EYE WEA MODELS is the device name listed in this FDA 510(k) record. The listed applicant is Apex Optical Ind. Co.. It received FDA 510(k) clearance on 1994-01-25 under 510(k) number K932821. 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 APEX OPTICAL IND. CO., EYE WEA MODELS?

APEX OPTICAL IND. CO., EYE WEA MODELS is a medical device that received FDA 510(k) clearance on 1994-01-25. The listed applicant is Apex Optical Ind. Co.. The 510(k) number is K932821.

When did APEX OPTICAL IND. CO., EYE WEA MODELS receive FDA 510(k) clearance?

APEX OPTICAL IND. CO., EYE WEA MODELS received FDA 510(k) clearance on 1994-01-25, under 510(k) number K932821.

Who is the listed applicant for APEX OPTICAL IND. CO., EYE WEA MODELS?

The FDA 510(k) record lists Apex Optical Ind. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for APEX OPTICAL IND. CO., EYE WEA MODELS?

The FDA product code for APEX OPTICAL IND. CO., EYE WEA MODELS is HQZ.

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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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