Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K060653
Device Classification Name
Powered Laser Surgical Instrument
More FDA Info for this Device
510(K) Number
K060653
Device Name
Powered Laser Surgical Instrument
Applicant
DERMACARE, INC.
6248 PRESTON AVENUE
LIVERMORE, CA 94551 US
Other 510(k) Applications for this Company
Contact
HEIDI STARK
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
03/13/2006
Decision Date
10/24/2006
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact