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FDA 510(k)

LABTICIAN RETINAL IMPLANTS

K-Number: K875014 · 1988-02-26

ApplicantLabtician Products, Inc.
Decision Date1988-02-26
Product CodeHQJ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LABTICIAN RETINAL IMPLANTS is the device name listed in this FDA 510(k) record. The listed applicant is Labtician Products, Inc.. It received FDA 510(k) clearance on 1988-02-26 under 510(k) number K875014. The device is classified under product code HQJ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LABTICIAN RETINAL IMPLANTS?

LABTICIAN RETINAL IMPLANTS is a medical device that received FDA 510(k) clearance on 1988-02-26. The listed applicant is Labtician Products, Inc.. The 510(k) number is K875014.

When did LABTICIAN RETINAL IMPLANTS receive FDA 510(k) clearance?

LABTICIAN RETINAL IMPLANTS received FDA 510(k) clearance on 1988-02-26, under 510(k) number K875014.

Who is the listed applicant for LABTICIAN RETINAL IMPLANTS?

The FDA 510(k) record lists Labtician Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LABTICIAN RETINAL IMPLANTS?

The FDA product code for LABTICIAN RETINAL IMPLANTS is HQJ.

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Related Devices (Code: HQJ)

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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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