FDA 510(k) Application Details - K223195

Device Classification Name	Sleeve, Limb, Compressible   More FDA Info for this Device
510(K) Number	K223195
Device Name	Sleeve, Limb, Compressible
Applicant	AIROS Medical, Inc 2501 Monroe Blvd. Suite 1200 Audubon, PA 19403 US Other 510(k) Applications for this Company
Contact	Darren Behuniak Other 510(k) Applications for this Contact
Regulation Number	870.5800   More FDA Info for this Regulation Number
Classification Product Code	JOW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/13/2022
Decision Date	12/09/2022
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review