LIQUIZYME CO2REAGENT SET
K-Number: K820388 · 1982-03-08
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Device Summary
Frequently Asked Questions
What is the LIQUIZYME CO2REAGENT SET?
LIQUIZYME CO2REAGENT SET is a medical device that received FDA 510(k) clearance on 1982-03-08. The listed applicant is American Research Products Co.. The 510(k) number is K820388.
When did LIQUIZYME CO2REAGENT SET receive FDA 510(k) clearance?
LIQUIZYME CO2REAGENT SET received FDA 510(k) clearance on 1982-03-08, under 510(k) number K820388.
Who is the listed applicant for LIQUIZYME CO2REAGENT 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 CO2REAGENT SET?
The FDA product code for LIQUIZYME CO2REAGENT SET is JFL.
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.
Related Devices (Code: JFL)
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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