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FDA 510(k)

OCTOPUS

K-Number: K780414 · 1978-04-10

ApplicantHitron Corp.
Decision Date1978-04-10
Product CodeHPT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OCTOPUS is the device name listed in this FDA 510(k) record. The listed applicant is Hitron Corp.. It received FDA 510(k) clearance on 1978-04-10 under 510(k) number K780414. 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?

OCTOPUS is a medical device that received FDA 510(k) clearance on 1978-04-10. The listed applicant is Hitron Corp.. The 510(k) number is K780414.

When did OCTOPUS receive FDA 510(k) clearance?

OCTOPUS received FDA 510(k) clearance on 1978-04-10, under 510(k) number K780414.

Who is the listed applicant for OCTOPUS?

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

What is the FDA product code for OCTOPUS?

The FDA product code for OCTOPUS is HPT.

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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.

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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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