Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K964070
Device Classification Name
Apparatus, Autotransfusion
More FDA Info for this Device
510(K) Number
K964070
Device Name
Apparatus, Autotransfusion
Applicant
DEKNATEL, INC.
49 PLAIN ST.
NORTH ATTLEBORO, MA 02760 US
Other 510(k) Applications for this Company
Contact
DIANE E MINEAR
Other 510(k) Applications for this Contact
Regulation Number
868.5830
More FDA Info for this Regulation Number
Classification Product Code
CAC
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
10/10/1996
Decision Date
12/31/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact