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FDA 510(k)

REFLAB(TM) BRAND SYST PK LIQ REAGENT, APOLIPOP A-1

K-Number: K914069 · 1991-10-02

Decision Date1991-10-02
Product CodeMSJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

REFLAB(TM) BRAND SYST PK LIQ REAGENT, APOLIPOP A-1 is the device name listed in this FDA 510(k) record. The listed applicant is Medical Analysis Systems, Inc.. It received FDA 510(k) clearance on 1991-10-02 under 510(k) number K914069. The device is classified under product code MSJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 107 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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