APHLELISA KIT— 510(k) K933588

Substantially Equivalent

Louisville Apl Diagnostics, Inc.

FDA 510(k) clearance K933588 for APHLELISA KIT, Substantially Equivalent on 1994-10-13. Applicant: Louisville Apl Diagnostics, Inc..

Clearance details

Applicant: Louisville Apl Diagnostics, Inc.
Product code: Code MID
Advisory panel: Immunology
Date received: 1993-07-26
Decision date: 1994-10-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Louisville, KY, US

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