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FDA 510(k)

ACCUMAP AUTOMATIC PERIMETER

K-Number: K022304 · 2003-11-14

ApplicantObjectivision Pty , Ltd.
Decision Date2003-11-14
Product CodeGWE
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ACCUMAP AUTOMATIC PERIMETER is the device name listed in this FDA 510(k) record. The listed applicant is Objectivision Pty , Ltd.. It received FDA 510(k) clearance on 2003-11-14 under 510(k) number K022304. The device is classified under product code GWE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCUMAP AUTOMATIC PERIMETER?

ACCUMAP AUTOMATIC PERIMETER is a medical device that received FDA 510(k) clearance on 2003-11-14. The listed applicant is Objectivision Pty , Ltd.. The 510(k) number is K022304.

When did ACCUMAP AUTOMATIC PERIMETER receive FDA 510(k) clearance?

ACCUMAP AUTOMATIC PERIMETER received FDA 510(k) clearance on 2003-11-14, under 510(k) number K022304.

Who is the listed applicant for ACCUMAP AUTOMATIC PERIMETER?

The FDA 510(k) record lists Objectivision Pty , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACCUMAP AUTOMATIC PERIMETER?

The FDA product code for ACCUMAP AUTOMATIC PERIMETER is GWE.

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Related Devices (Code: GWE)

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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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