Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K011373
Device Classification Name
Trocar
More FDA Info for this Device
510(K) Number
K011373
Device Name
Trocar
Applicant
MEDCANICA, INC.
19526 EAST LAKE DR.
MIAMI, FL 33015 US
Other 510(k) Applications for this Company
Contact
AL WEISENBORN
Other 510(k) Applications for this Contact
Regulation Number
870.1390
More FDA Info for this Regulation Number
Classification Product Code
DRC
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
05/04/2001
Decision Date
10/12/2001
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact