LIQUIZYME TOTAL PROTEIN REAGENT
K-Number: K823170 · 1982-11-29
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Device Summary
Frequently Asked Questions
What is the LIQUIZYME TOTAL PROTEIN REAGENT?
LIQUIZYME TOTAL PROTEIN REAGENT is a medical device that received FDA 510(k) clearance on 1982-11-29. The listed applicant is Amresco, Inc.. The 510(k) number is K823170.
When did LIQUIZYME TOTAL PROTEIN REAGENT receive FDA 510(k) clearance?
LIQUIZYME TOTAL PROTEIN REAGENT received FDA 510(k) clearance on 1982-11-29, under 510(k) number K823170.
Who is the listed applicant for LIQUIZYME TOTAL PROTEIN REAGENT?
The FDA 510(k) record lists Amresco, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIQUIZYME TOTAL PROTEIN REAGENT?
The FDA product code for LIQUIZYME TOTAL PROTEIN REAGENT is CEK.
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 Amresco, Inc. 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: CEK)
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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