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FDA 510(k)

AUTO PERIOMETER 3000

K-Number: K822580 · 1982-09-30

ApplicantDicon, Inc.
Decision Date1982-09-30
Product CodeHPT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

AUTO PERIOMETER 3000 is the device name listed in this FDA 510(k) record. The listed applicant is Dicon, Inc.. It received FDA 510(k) clearance on 1982-09-30 under 510(k) number K822580. 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 AUTO PERIOMETER 3000?

AUTO PERIOMETER 3000 is a medical device that received FDA 510(k) clearance on 1982-09-30. The listed applicant is Dicon, Inc.. The 510(k) number is K822580.

When did AUTO PERIOMETER 3000 receive FDA 510(k) clearance?

AUTO PERIOMETER 3000 received FDA 510(k) clearance on 1982-09-30, under 510(k) number K822580.

Who is the listed applicant for AUTO PERIOMETER 3000?

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

What is the FDA product code for AUTO PERIOMETER 3000?

The FDA product code for AUTO PERIOMETER 3000 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Dicon, 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.

K820877AUTOMATIC OBJECTIVE REFRACTOR 2000K811347DICON AUTO PERIMETER 2000K811346DICON AUTO PERIMETER 200

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

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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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