Dayspring— 510(k) K223228

Substantially Equivalent

Koya Medical, Inc.

FDA 510(k) clearance K223228 for Dayspring, Substantially Equivalent on 2024-01-04. Applicant: Koya Medical, Inc..

Clearance details

Applicant: Koya Medical, Inc.
Product code: Code JOW
Advisory panel: Cardiovascular
Date received: 2022-10-18
Decision date: 2024-01-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oakland, CA, US

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