AnemoCheck Home— 510(k) K221508

Substantially Equivalent

Sanguina, Inc.

FDA 510(k) clearance K221508 for AnemoCheck Home, Substantially Equivalent on 2023-09-29. Applicant: Sanguina, Inc..

Clearance details

Applicant: Sanguina, Inc.
Product code: Code KHG
Advisory panel: Hematology
Date received: 2022-05-24
Decision date: 2023-09-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Peachtree Corners, GA, US

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