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FDA 510(k)

LIQUIZYME CALCIUM REAGENT SET

K-Number: K823219 · 1982-12-03

Decision Date1982-12-03
Product CodeCIC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIQUIZYME CALCIUM REAGENT SET is the device name listed in this FDA 510(k) record. The listed applicant is American Research Products Co.. It received FDA 510(k) clearance on 1982-12-03 under 510(k) number K823219. The device is classified under product code CIC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUIZYME CALCIUM REAGENT SET?

LIQUIZYME CALCIUM REAGENT SET is a medical device that received FDA 510(k) clearance on 1982-12-03. The listed applicant is American Research Products Co.. The 510(k) number is K823219.

When did LIQUIZYME CALCIUM REAGENT SET receive FDA 510(k) clearance?

LIQUIZYME CALCIUM REAGENT SET received FDA 510(k) clearance on 1982-12-03, under 510(k) number K823219.

Who is the listed applicant for LIQUIZYME CALCIUM REAGENT SET?

The FDA 510(k) record lists American Research Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIQUIZYME CALCIUM REAGENT SET?

The FDA product code for LIQUIZYME CALCIUM REAGENT SET is CIC.

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 American Research Products Co. 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.

View all 56 devices →

Related Devices (Code: CIC)

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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