Apo A-I Ria Kit-Human Plasma Apolip-

FDA 510(k) K840105 · Iso-Tex Diagnostics

Unknown

510(k) numberK840105

Submission

Device name
Apo A-I Ria Kit-Human Plasma Apolip-
Applicant
Iso-Tex Diagnostics
Mchenry, IL, US
Received
January 10, 1984
Decision date
January 10, 1984
Decision
Unknown (SESP)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

No product code recorded.

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Questions and answers

When was Apo A-I Ria Kit-Human Plasma Apolip- cleared by the FDA?

Apo A-I Ria Kit-Human Plasma Apolip- (K840105) received a 510(k) decision of Unknown on January 10, 1984, 0 days after the submission was received.