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FDA 510(k)

AUTO-FIELD D AUTOMATED VISUAL DETECTOR

K-Number: K800722 · 1980-04-29

ApplicantCavitron Corp.
Decision Date1980-04-29
Product CodeHPT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

AUTO-FIELD D AUTOMATED VISUAL DETECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Cavitron Corp.. It received FDA 510(k) clearance on 1980-04-29 under 510(k) number K800722. 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 D AUTOMATED VISUAL DETECTOR?

AUTO-FIELD D AUTOMATED VISUAL DETECTOR is a medical device that received FDA 510(k) clearance on 1980-04-29. The listed applicant is Cavitron Corp.. The 510(k) number is K800722.

When did AUTO-FIELD D AUTOMATED VISUAL DETECTOR receive FDA 510(k) clearance?

AUTO-FIELD D AUTOMATED VISUAL DETECTOR received FDA 510(k) clearance on 1980-04-29, under 510(k) number K800722.

Who is the listed applicant for AUTO-FIELD D AUTOMATED VISUAL DETECTOR?

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 D AUTOMATED VISUAL DETECTOR?

The FDA product code for AUTO-FIELD D AUTOMATED VISUAL DETECTOR 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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