ANEMIAPRO SELF-SCREENER— 510(k) K042379

Substantially Equivalent

Biosafe Laboratories, Inc.

FDA 510(k) clearance K042379 for ANEMIAPRO SELF-SCREENER, Substantially Equivalent on 2004-12-15. Applicant: Biosafe Laboratories, Inc..

Clearance details

Applicant: Biosafe Laboratories, Inc.
Product code: Code KHG
Advisory panel: Hematology
Date received: 2004-09-01
Decision date: 2004-12-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Forest, IL, US

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