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FDA 510(k)

AUTO-FIELD II OPHTHALMIC FIELD SCANNER

K-Number: K781462 · 1978-09-14

ApplicantCavitron Corp.
Decision Date1978-09-14
Product CodeHPT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

AUTO-FIELD II OPHTHALMIC FIELD SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is Cavitron Corp.. It received FDA 510(k) clearance on 1978-09-14 under 510(k) number K781462. 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-FIELD II OPHTHALMIC FIELD SCANNER?

AUTO-FIELD II OPHTHALMIC FIELD SCANNER is a medical device that received FDA 510(k) clearance on 1978-09-14. The listed applicant is Cavitron Corp.. The 510(k) number is K781462.

When did AUTO-FIELD II OPHTHALMIC FIELD SCANNER receive FDA 510(k) clearance?

AUTO-FIELD II OPHTHALMIC FIELD SCANNER received FDA 510(k) clearance on 1978-09-14, under 510(k) number K781462.

Who is the listed applicant for AUTO-FIELD II OPHTHALMIC FIELD SCANNER?

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

What is the FDA product code for AUTO-FIELD II OPHTHALMIC FIELD SCANNER?

The FDA product code for AUTO-FIELD II OPHTHALMIC FIELD SCANNER is HPT.

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Other records listing Cavitron Corp. 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.

K811582THE PLACERK810207MINOR SURGERY LIGHTK802928SPIROMETRIC COMPUTER #SC-10K801623CAVITRON ULTRASONIC SURG. ASPIR. CUSAK801877SLIT LAMP ATTACHMENTK800869MODEL PM-20(N)(R)CO2 PATIENT MONITOR/ALA

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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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