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FDA 510(k)

FORESEE HOME

K-Number: K091579 · 2009-12-23

ApplicantNotal Vision , Ltd.
Decision Date2009-12-23
Product CodeHPT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

FORESEE HOME is the device name listed in this FDA 510(k) record. The listed applicant is Notal Vision , Ltd.. It received FDA 510(k) clearance on 2009-12-23 under 510(k) number K091579. The device is classified under product code HPT. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORESEE HOME?

FORESEE HOME is a medical device that received FDA 510(k) clearance on 2009-12-23. The listed applicant is Notal Vision , Ltd.. The 510(k) number is K091579.

When did FORESEE HOME receive FDA 510(k) clearance?

FORESEE HOME received FDA 510(k) clearance on 2009-12-23, under 510(k) number K091579.

Who is the listed applicant for FORESEE HOME?

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

What is the FDA product code for FORESEE HOME?

The FDA product code for FORESEE HOME is HPT.

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Related Devices (Code: HPT)

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.

K092187MAIA, MODEL 1Centervue S.P.A.K093213GUIDED PROGRESSION ANALYSIS ON THE HUMPHREY FIELD ANALYZER II AND II -I SERIESCarl Zeiss Meditec, Inc.K063310TRUEFIELD ANALYZERSeeing Machines LimitedK050350THE NOTAL VISION PREVIEW PREFERENTIAL HYPERACUITY PERIMETER (PREVIEW PHP)Notal Vision, Inc.K023623NOVAVISION, MODEL 2.0Novavision, Inc.K971156KASHA VISUAL FIELD SYSTEMKasha Software, Inc.

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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