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FDA 510(k)

LIQUIZYME TOTAL PROTEIN REAGENT

K-Number: K823170 · 1982-11-29

ApplicantAmresco, Inc.
Decision Date1982-11-29
Product CodeCEK
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIQUIZYME TOTAL PROTEIN REAGENT is the device name listed in this FDA 510(k) record. The listed applicant is Amresco, Inc.. It received FDA 510(k) clearance on 1982-11-29 under 510(k) number K823170. The device is classified under product code CEK. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

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.

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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

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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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