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FDA 510(k)

LAS-R HUMAN PREALBUMIN TEST

K-Number: K772329 · 1978-02-03

ApplicantHyland Therapeutic Div., Travenol Laboratories
Decision Date1978-02-03
Product CodeJZJ
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

LAS-R HUMAN PREALBUMIN TEST is the device name listed in this FDA 510(k) record. The listed applicant is Hyland Therapeutic Div., Travenol Laboratories. It received FDA 510(k) clearance on 1978-02-03 under 510(k) number K772329. The device is classified under product code JZJ. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAS-R HUMAN PREALBUMIN TEST?

LAS-R HUMAN PREALBUMIN TEST is a medical device that received FDA 510(k) clearance on 1978-02-03. The listed applicant is Hyland Therapeutic Div., Travenol Laboratories. The 510(k) number is K772329.

When did LAS-R HUMAN PREALBUMIN TEST receive FDA 510(k) clearance?

LAS-R HUMAN PREALBUMIN TEST received FDA 510(k) clearance on 1978-02-03, under 510(k) number K772329.

Who is the listed applicant for LAS-R HUMAN PREALBUMIN TEST?

The FDA 510(k) record lists Hyland Therapeutic Div., Travenol Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAS-R HUMAN PREALBUMIN TEST?

The FDA product code for LAS-R HUMAN PREALBUMIN TEST is JZJ.

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Related Devices (Code: JZJ)

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

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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