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FDA 510(k)

LIQUIZYME NA+/K+ REAGENT SET

K-Number: K820395 · 1982-03-11

Decision Date1982-03-11
Product CodeJGS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIQUIZYME NA+/K+ 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 1982-03-11 under 510(k) number K820395. The device is classified under product code JGS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUIZYME NA+/K+ REAGENT SET?

LIQUIZYME NA+/K+ REAGENT SET is a medical device that received FDA 510(k) clearance on 1982-03-11. The listed applicant is American Research Products Co.. The 510(k) number is K820395.

When did LIQUIZYME NA+/K+ REAGENT SET receive FDA 510(k) clearance?

LIQUIZYME NA+/K+ REAGENT SET received FDA 510(k) clearance on 1982-03-11, under 510(k) number K820395.

Who is the listed applicant for LIQUIZYME NA+/K+ 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 NA+/K+ REAGENT SET?

The FDA product code for LIQUIZYME NA+/K+ REAGENT SET is JGS.

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: JGS)

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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