Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K033179
Device Classification Name
Pump, Portable, Aspiration (Manual Or Powered)
More FDA Info for this Device
510(K) Number
K033179
Device Name
Pump, Portable, Aspiration (Manual Or Powered)
Applicant
MEDELA AG
LAETTICHSTRASSE 4
CH-6340 BAAR CH
Other 510(k) Applications for this Company
Contact
WERNER FREI
Other 510(k) Applications for this Contact
Regulation Number
878.4780
More FDA Info for this Regulation Number
Classification Product Code
BTA
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
10/01/2003
Decision Date
10/15/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Abbreviated
Reviewed By Third Party
Y
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact