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FDA 510(k)

THE HUMPHREY FIELD ANALYZER MODEL 610

K-Number: K821940 · 1982-07-28

ApplicantZeiss Humphrey System
Decision Date1982-07-28
Product CodeHPT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

THE HUMPHREY FIELD ANALYZER MODEL 610 is the device name listed in this FDA 510(k) record. The listed applicant is Zeiss Humphrey System. It received FDA 510(k) clearance on 1982-07-28 under 510(k) number K821940. 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 THE HUMPHREY FIELD ANALYZER MODEL 610?

THE HUMPHREY FIELD ANALYZER MODEL 610 is a medical device that received FDA 510(k) clearance on 1982-07-28. The listed applicant is Zeiss Humphrey System. The 510(k) number is K821940.

When did THE HUMPHREY FIELD ANALYZER MODEL 610 receive FDA 510(k) clearance?

THE HUMPHREY FIELD ANALYZER MODEL 610 received FDA 510(k) clearance on 1982-07-28, under 510(k) number K821940.

Who is the listed applicant for THE HUMPHREY FIELD ANALYZER MODEL 610?

The FDA 510(k) record lists Zeiss Humphrey System as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE HUMPHREY FIELD ANALYZER MODEL 610?

The FDA product code for THE HUMPHREY FIELD ANALYZER MODEL 610 is HPT.

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Other records listing Zeiss Humphrey System 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.

K942439ZEISS OPMILAS 144 SURGICAL LASERSK923211DIGITAL OPHTHALMIC ULTRASOUND BIOMICROSCOPEK923348OPHTHALMIC A/B SCAN SYSTEM, MODEL 835 -- MODIFIEDK852639HUMPHREY FIELD ANALYZER MODEL 630K852638HUMPHREY IMAGE ANALYZER MODEL 110K802029OBJECTIVE REFRACTOR

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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.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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