Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K024088
Device Classification Name
Powered Laser Surgical Instrument
More FDA Info for this Device
510(K) Number
K024088
Device Name
Powered Laser Surgical Instrument
Applicant
BIOLITEC, INC.
555 THIRTEENTH ST., NW
WASHINGTON, DC 20004-5910 US
Other 510(k) Applications for this Company
Contact
JONATHAN S KAHAN
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
12/11/2002
Decision Date
01/02/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact