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FDA 510(k)

COMPUTERIZED TOMOGRAPHY-HYPERBARIC OXYG

K-Number: K831888 · 1983-07-12

ApplicantPortable Travtion Device Co.
Decision Date1983-07-12
Product CodeHST
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

COMPUTERIZED TOMOGRAPHY-HYPERBARIC OXYG is the device name listed in this FDA 510(k) record. The listed applicant is Portable Travtion Device Co.. It received FDA 510(k) clearance on 1983-07-12 under 510(k) number K831888. The device is classified under product code HST. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPUTERIZED TOMOGRAPHY-HYPERBARIC OXYG?

COMPUTERIZED TOMOGRAPHY-HYPERBARIC OXYG is a medical device that received FDA 510(k) clearance on 1983-07-12. The listed applicant is Portable Travtion Device Co.. The 510(k) number is K831888.

When did COMPUTERIZED TOMOGRAPHY-HYPERBARIC OXYG receive FDA 510(k) clearance?

COMPUTERIZED TOMOGRAPHY-HYPERBARIC OXYG received FDA 510(k) clearance on 1983-07-12, under 510(k) number K831888.

Who is the listed applicant for COMPUTERIZED TOMOGRAPHY-HYPERBARIC OXYG?

The FDA 510(k) record lists Portable Travtion Device Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COMPUTERIZED TOMOGRAPHY-HYPERBARIC OXYG?

The FDA product code for COMPUTERIZED TOMOGRAPHY-HYPERBARIC OXYG is HST.

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Related Devices (Code: HST)

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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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