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FDA 510(k)

TKS 4000 AUTO PERIMETER

K-Number: K873122 · 1987-11-02

ApplicantVismed, Inc.
Decision Date1987-11-02
Product CodeHPT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

TKS 4000 AUTO PERIMETER is the device name listed in this FDA 510(k) record. The listed applicant is Vismed, Inc.. It received FDA 510(k) clearance on 1987-11-02 under 510(k) number K873122. 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 TKS 4000 AUTO PERIMETER?

TKS 4000 AUTO PERIMETER is a medical device that received FDA 510(k) clearance on 1987-11-02. The listed applicant is Vismed, Inc.. The 510(k) number is K873122.

When did TKS 4000 AUTO PERIMETER receive FDA 510(k) clearance?

TKS 4000 AUTO PERIMETER received FDA 510(k) clearance on 1987-11-02, under 510(k) number K873122.

Who is the listed applicant for TKS 4000 AUTO PERIMETER?

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

What is the FDA product code for TKS 4000 AUTO PERIMETER?

The FDA product code for TKS 4000 AUTO PERIMETER is HPT.

Related Clinical Trials

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.

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Other records listing Vismed, Inc. as applicant

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.

K930937LD 400

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.K091579FORESEE HOMENotal Vision , Ltd.K063310TRUEFIELD ANALYZERSeeing Machines LimitedK050350THE NOTAL VISION PREVIEW PREFERENTIAL HYPERACUITY PERIMETER (PREVIEW PHP)Notal Vision, Inc.K023623NOVAVISION, MODEL 2.0Novavision, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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