Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K020154
Device Classification Name
Device, External Penile Rigidity
More FDA Info for this Device
510(K) Number
K020154
Device Name
Device, External Penile Rigidity
Applicant
POS-T-VAC, INC.
1701 NORTH 14TH AVE.
DODGE CITY, KS 67801 US
Other 510(k) Applications for this Company
Contact
DENNIS L BELL
Other 510(k) Applications for this Contact
Regulation Number
876.5020
More FDA Info for this Regulation Number
Classification Product Code
LKY
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
01/17/2002
Decision Date
04/04/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
GU - Gastroenterology & Urology
Review Advisory Committee
GU - Gastroenterology & Urology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact