Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K122358
Device Classification Name
Powered Laser Surgical Instrument
More FDA Info for this Device
510(K) Number
K122358
Device Name
Powered Laser Surgical Instrument
Applicant
HOGAN LOVELLS US, L.L.P.
1835 MARKET STREET
29TH FLOOR
PHILIDELPHIA, PA 19103 US
Other 510(k) Applications for this Company
Contact
JANICE HOGAN
Other 510(k) Applications for this Contact
Regulation Number
878.4810
More FDA Info for this Regulation Number
Classification Product Code
GEX
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
08/03/2012
Decision Date
03/11/2014
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact