Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K955732
Device Classification Name
Set, Administration, Intravascular
More FDA Info for this Device
510(K) Number
K955732
Device Name
Set, Administration, Intravascular
Applicant
DISTRONIC STERILE PRODUCTS, INC.
124 HERITAGE AVE.
PORTSMOUTH, NH 03801-5645 US
Other 510(k) Applications for this Company
Contact
JOYCE MCDOUGAL
Other 510(k) Applications for this Contact
Regulation Number
880.5440
More FDA Info for this Regulation Number
Classification Product Code
FPA
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
12/19/1995
Decision Date
02/21/1996
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