REFLAB(TM) BRAND SYST PK LIQ REAGENT, APOLIPOP A-1
K-Number: K914069 · 1991-10-02
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Device Summary
Frequently Asked Questions
What is the REFLAB(TM) BRAND SYST PK LIQ REAGENT, APOLIPOP A-1?
REFLAB(TM) BRAND SYST PK LIQ REAGENT, APOLIPOP A-1 is a medical device that received FDA 510(k) clearance on 1991-10-02. The listed applicant is Medical Analysis Systems, Inc.. The 510(k) number is K914069.
When did REFLAB(TM) BRAND SYST PK LIQ REAGENT, APOLIPOP A-1 receive FDA 510(k) clearance?
REFLAB(TM) BRAND SYST PK LIQ REAGENT, APOLIPOP A-1 received FDA 510(k) clearance on 1991-10-02, under 510(k) number K914069.
Who is the listed applicant for REFLAB(TM) BRAND SYST PK LIQ REAGENT, APOLIPOP A-1?
The FDA 510(k) record lists Medical Analysis Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for REFLAB(TM) BRAND SYST PK LIQ REAGENT, APOLIPOP A-1?
The FDA product code for REFLAB(TM) BRAND SYST PK LIQ REAGENT, APOLIPOP A-1 is MSJ.
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 Medical Analysis Systems, 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: MSJ)
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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