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FDA 510(k)

ANISEIKONIA INSPECTOR

K-Number: K013110 · 2001-12-19

ApplicantOptical Diagnostics, Inc.
Decision Date2001-12-19
Product CodeHJT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ANISEIKONIA INSPECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Optical Diagnostics, Inc.. It received FDA 510(k) clearance on 2001-12-19 under 510(k) number K013110. The device is classified under product code HJT. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANISEIKONIA INSPECTOR?

ANISEIKONIA INSPECTOR is a medical device that received FDA 510(k) clearance on 2001-12-19. The listed applicant is Optical Diagnostics, Inc.. The 510(k) number is K013110.

When did ANISEIKONIA INSPECTOR receive FDA 510(k) clearance?

ANISEIKONIA INSPECTOR received FDA 510(k) clearance on 2001-12-19, under 510(k) number K013110.

Who is the listed applicant for ANISEIKONIA INSPECTOR?

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

What is the FDA product code for ANISEIKONIA INSPECTOR?

The FDA product code for ANISEIKONIA INSPECTOR is HJT.

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Related Devices (Code: HJT)

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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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