Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K101412
Device Classification Name
Container, I.V.
More FDA Info for this Device
510(K) Number
K101412
Device Name
Container, I.V.
Applicant
VALMED S.R.L.
VIA PROVINCIALE 10
MAZZO DI VALTELLINA SO I 23030 IT
Other 510(k) Applications for this Company
Contact
WALTER SVANOSIO
Other 510(k) Applications for this Contact
Regulation Number
880.5025
More FDA Info for this Regulation Number
Classification Product Code
KPE
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
05/20/2010
Decision Date
04/13/2011
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
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact