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FDA 510(k)

OPTIFIELD I AND II AUTOMATED PERIMETERS

K-Number: K884867 · 1989-03-09

ApplicantOptimed, Inc.
Decision Date1989-03-09
Product CodeHPT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OPTIFIELD I AND II AUTOMATED PERIMETERS is the device name listed in this FDA 510(k) record. The listed applicant is Optimed, Inc.. It received FDA 510(k) clearance on 1989-03-09 under 510(k) number K884867. 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 OPTIFIELD I AND II AUTOMATED PERIMETERS?

OPTIFIELD I AND II AUTOMATED PERIMETERS is a medical device that received FDA 510(k) clearance on 1989-03-09. The listed applicant is Optimed, Inc.. The 510(k) number is K884867.

When did OPTIFIELD I AND II AUTOMATED PERIMETERS receive FDA 510(k) clearance?

OPTIFIELD I AND II AUTOMATED PERIMETERS received FDA 510(k) clearance on 1989-03-09, under 510(k) number K884867.

Who is the listed applicant for OPTIFIELD I AND II AUTOMATED PERIMETERS?

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

What is the FDA product code for OPTIFIELD I AND II AUTOMATED PERIMETERS?

The FDA product code for OPTIFIELD I AND II AUTOMATED PERIMETERS 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 Optimed, 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.

K903462OPTIMED GLAUCOMA PRESSURE REGULATORK890687ECT-100 ELECTRONIC CORNEAL TOPOGRAPHERK883458OPTIMED ADVANTAGE

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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