LAS-R HUMAN IGD TEST
K-Number: K772327 · 1978-02-28
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Device Summary
Frequently Asked Questions
What is the LAS-R HUMAN IGD TEST?
LAS-R HUMAN IGD TEST is a medical device that received FDA 510(k) clearance on 1978-02-28. The listed applicant is Hyland Therapeutic Div., Travenol Laboratories. The 510(k) number is K772327.
When did LAS-R HUMAN IGD TEST receive FDA 510(k) clearance?
LAS-R HUMAN IGD TEST received FDA 510(k) clearance on 1978-02-28, under 510(k) number K772327.
Who is the listed applicant for LAS-R HUMAN IGD 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 IGD TEST?
The FDA product code for LAS-R HUMAN IGD TEST is CZJ.
Related Clinical Trials
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.
Other records listing Hyland Therapeutic Div., Travenol Laboratories 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.
Related Devices (Code: CZJ)
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.
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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