LIQUID AST (SGOT)REAGENT SET
K-Number: K941132 · 1994-05-02
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Device Summary
Frequently Asked Questions
What is the LIQUID AST (SGOT)REAGENT SET?
LIQUID AST (SGOT)REAGENT SET is a medical device that received FDA 510(k) clearance on 1994-05-02. The listed applicant is Pointe Scientific, Inc.,. The 510(k) number is K941132.
When did LIQUID AST (SGOT)REAGENT SET receive FDA 510(k) clearance?
LIQUID AST (SGOT)REAGENT SET received FDA 510(k) clearance on 1994-05-02, under 510(k) number K941132.
Who is the listed applicant for LIQUID AST (SGOT)REAGENT SET?
The FDA 510(k) record lists Pointe Scientific, Inc., as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIQUID AST (SGOT)REAGENT SET?
The FDA product code for LIQUID AST (SGOT)REAGENT SET is CIT.
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 Pointe Scientific, 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.
Related Devices (Code: CIT)
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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