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FDA 510(k)

CUSTOM ARTIFICIAL HUMAN EYES

K-Number: K945270 · 1995-05-30

ApplicantDaniel T Acosta
Decision Date1995-05-30
Product CodeHQH
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CUSTOM ARTIFICIAL HUMAN EYES is the device name listed in this FDA 510(k) record. The listed applicant is Daniel T Acosta. It received FDA 510(k) clearance on 1995-05-30 under 510(k) number K945270. The device is classified under product code HQH. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUSTOM ARTIFICIAL HUMAN EYES?

CUSTOM ARTIFICIAL HUMAN EYES is a medical device that received FDA 510(k) clearance on 1995-05-30. The listed applicant is Daniel T Acosta. The 510(k) number is K945270.

When did CUSTOM ARTIFICIAL HUMAN EYES receive FDA 510(k) clearance?

CUSTOM ARTIFICIAL HUMAN EYES received FDA 510(k) clearance on 1995-05-30, under 510(k) number K945270.

Who is the listed applicant for CUSTOM ARTIFICIAL HUMAN EYES?

The FDA 510(k) record lists Daniel T Acosta as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CUSTOM ARTIFICIAL HUMAN EYES?

The FDA product code for CUSTOM ARTIFICIAL HUMAN EYES is HQH.

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Related Devices (Code: HQH)

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.

K952538ROBERT B. SCOTT PLASTIC ARTIFICALRobert B. Scott Ocularists of Florida, Inc.K946226CUSTOM OCULAR PROSTHESISFrank Tanaka, Ocularist, Inc.K923167THE NISSEL ARTIFICIAL EYENissel , Ltd.K904962EYE ARTIFICIAL CUSTOMMidwest Eye Laboratories, Inc.K791923SCLERAL POWDEROcularists , Ltd.

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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