Reflab(Tm) Brand Syst PK Liq Reagent, Apolipop A-1

FDA 510(k) K914069 · Medical Analysis Systems, Inc.

Substantially Equivalent

510(k) numberK914069

Submission

Device name
Reflab(Tm) Brand Syst PK Liq Reagent, Apolipop A-1
Applicant
Medical Analysis Systems, Inc.
Camarillo, CA, US
Received
September 11, 1991
Decision date
October 2, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
MSJ – Apolipoproteins
Device class
Class I (low risk)
Regulation
21 CFR 862.1475
Specialty
Clinical Chemistry

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K931777Apo A-1 Chemiluminescence AssayMSJ · Traditional Nichols Institute08/16/1993SE
K925702Nichols Apo B Chemiluminescence AssayMSJ · Traditional Nichols Institute Diagnostics12/23/1992SE
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Questions and answers

When was Reflab(Tm) Brand Syst PK Liq Reagent, Apolipop A-1 cleared by the FDA?

Reflab(Tm) Brand Syst PK Liq Reagent, Apolipop A-1 (K914069) received a 510(k) decision of Substantially Equivalent on October 2, 1991, 21 days after the submission was received.

What is the product code of K914069?

The FDA product code is MSJ – Apolipoproteins, a Class I (low risk) device regulated under 21 CFR 862.1475.