FDA 510(k) Application Details - K240125

Device Classification Name	Sleeve, Limb, Compressible   More FDA Info for this Device
510(K) Number	K240125
Device Name	Sleeve, Limb, Compressible
Applicant	Zenith Technical Innovations 1396 St. Paul Ave. Gurnee, IL 60031 US Other 510(k) Applications for this Company
Contact	Greg Binversie 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	01/16/2024
Decision Date	06/21/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review