FDA 510(k) Application Details - K220565

Device Classification Name	Spirometer, Therapeutic (Incentive)   More FDA Info for this Device
510(K) Number	K220565
Device Name	Spirometer, Therapeutic (Incentive)
Applicant	Medline Industries, Inc. 1 Three Lakes Drive Northfield, IL 60093 US Other 510(k) Applications for this Company
Contact	Nicole Schaffer Other 510(k) Applications for this Contact
Regulation Number	868.5690   More FDA Info for this Regulation Number
Classification Product Code	BWF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/28/2022
Decision Date	10/25/2022
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review