LKW — Laser, Neurosurgical Class III

FDA Device Classification

FDA product code LKW covers "Laser, Neurosurgical", a Class III medical device. Submissions are reviewed by the Unknown panel. At least 5 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
LKW
Device Class
Class III
Regulation Number
Submission Type
Review Panel
NE
Medical Specialty
Unknown
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K875042surgilaseND:YAG 100 SURGICAL LASER FOR NEURO & PULMONARYJune 24, 1988
K880172cooper lasersonicsMODEL 4900 ND:YAG LASER FOR NEUROSURGERY APPLICA.March 11, 1988
K864166weck surgical systems25 WATT CARBON DIOXIDE MEDICAL LASER FOR NEUROLOGYFebruary 10, 1987
K853580endo laseMEDILAS 2February 13, 1986
K844440cooper lasersonicsMODEL 4000 ND:YAG LASER FOR HEMORRHAGE CONTROLMay 9, 1985