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FDA 510(k)

OCTOPUS 500/500E

K-Number: K841099 · 1984-06-19

ApplicantCilco, Inc.
Decision Date1984-06-19
Product CodeHPT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OCTOPUS 500/500E is the device name listed in this FDA 510(k) record. The listed applicant is Cilco, Inc.. It received FDA 510(k) clearance on 1984-06-19 under 510(k) number K841099. 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 OCTOPUS 500/500E?

OCTOPUS 500/500E is a medical device that received FDA 510(k) clearance on 1984-06-19. The listed applicant is Cilco, Inc.. The 510(k) number is K841099.

When did OCTOPUS 500/500E receive FDA 510(k) clearance?

OCTOPUS 500/500E received FDA 510(k) clearance on 1984-06-19, under 510(k) number K841099.

Who is the listed applicant for OCTOPUS 500/500E?

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

What is the FDA product code for OCTOPUS 500/500E?

The FDA product code for OCTOPUS 500/500E is HPT.

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Other records listing Cilco, 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.

K861334CILCO DIAMOND KNIVES & DIAMOND KNIFE LINEAR GAUGEK854969CILCO SONOMETRICS A&B DIGITAL SYSTEM (DIGISCAN)K844249K-SOLK843319CILCO I/A SURGICAL PACKK843992CILCOR OPHTHALMIC INSTRUMENTSK843447CILCO DIAMOND KNIFE

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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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