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FDA 510(k)

HILO TRANS-X TRAUMA TRANSPORT

K-Number: K792326 · 1980-01-28

ApplicantTecnomed, Inc.
Decision Date1980-01-28
Product CodeIXR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HILO TRANS-X TRAUMA TRANSPORT is the device name listed in this FDA 510(k) record. The listed applicant is Tecnomed, Inc.. It received FDA 510(k) clearance on 1980-01-28 under 510(k) number K792326. The device is classified under product code IXR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HILO TRANS-X TRAUMA TRANSPORT?

HILO TRANS-X TRAUMA TRANSPORT is a medical device that received FDA 510(k) clearance on 1980-01-28. The listed applicant is Tecnomed, Inc.. The 510(k) number is K792326.

When did HILO TRANS-X TRAUMA TRANSPORT receive FDA 510(k) clearance?

HILO TRANS-X TRAUMA TRANSPORT received FDA 510(k) clearance on 1980-01-28, under 510(k) number K792326.

Who is the listed applicant for HILO TRANS-X TRAUMA TRANSPORT?

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

What is the FDA product code for HILO TRANS-X TRAUMA TRANSPORT?

The FDA product code for HILO TRANS-X TRAUMA TRANSPORT is IXR.

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Related Devices (Code: IXR)

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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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