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FDA 510(k)

PANORAMIC, MODEL 200MA

K-Number: K060424 · 2006-03-17

ApplicantOptos Plc.
Decision Date2006-03-17
Product CodeMYC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PANORAMIC, MODEL 200MA is the device name listed in this FDA 510(k) record. The listed applicant is Optos Plc.. It received FDA 510(k) clearance on 2006-03-17 under 510(k) number K060424. The device is classified under product code MYC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PANORAMIC, MODEL 200MA?

PANORAMIC, MODEL 200MA is a medical device that received FDA 510(k) clearance on 2006-03-17. The listed applicant is Optos Plc.. The 510(k) number is K060424.

When did PANORAMIC, MODEL 200MA receive FDA 510(k) clearance?

PANORAMIC, MODEL 200MA received FDA 510(k) clearance on 2006-03-17, under 510(k) number K060424.

Who is the listed applicant for PANORAMIC, MODEL 200MA?

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

What is the FDA product code for PANORAMIC, MODEL 200MA?

The FDA product code for PANORAMIC, MODEL 200MA is MYC.

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Other records listing Optos Plc. 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.

K233602P200TE (A10700)K231673P200TE (A10700)K190732P200TxEK173707P200TEK162039OptosAdvance 4.0 SoftwareK121043OPTOS OCT/SLO MICROPERIMETER

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Related Devices (Code: MYC)

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.

K261255KOWA FM-600Kowa Company, Ltd. Chofu FactoryK241931OcuMet Beacon (OCUB100)Ocusciences, Inc.K243504MAIA (AHMACME001)Centervue S.P.A.K213705DRSplusCentervue S.P.A.K211328EIDON FA, EIDON, EIDON AF, EIDON UWFLCentervue S.P.A.K192113DRSplusCentervue S.P.A.

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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