CK REAGENT
K-Number: K971396 · 1997-05-29
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Device Summary
Frequently Asked Questions
What is the CK REAGENT?
CK REAGENT is a medical device that received FDA 510(k) clearance on 1997-05-29. The listed applicant is Carolina Liquid Chemistries Corp.. The 510(k) number is K971396.
When did CK REAGENT receive FDA 510(k) clearance?
CK REAGENT received FDA 510(k) clearance on 1997-05-29, under 510(k) number K971396.
Who is the listed applicant for CK REAGENT?
The FDA 510(k) record lists Carolina Liquid Chemistries Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CK REAGENT?
The FDA product code for CK REAGENT is CGS.
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 Carolina Liquid Chemistries Corp. 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: CGS)
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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