Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K170218
Device Classification Name
Syringe, Piston
More FDA Info for this Device
510(K) Number
K170218
Device Name
Syringe, Piston
Applicant
Vesco Medical, LLC
692 N. High Street, Suite 205
Columbus, OH 43215 US
Other 510(k) Applications for this Company
Contact
Chris O'Keefe
Other 510(k) Applications for this Contact
Regulation Number
880.5860
More FDA Info for this Regulation Number
Classification Product Code
FMF
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
01/25/2017
Decision Date
02/24/2017
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
Y
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact