510(k) K924348

AD-TECH'S BRAIN BIOPSY NEEDLE FOR STEREOTAXIC by Ad-Tech Medical Instrument Corp — Product Code HAW

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 23, 1992
Date Received
August 27, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Neurological Stereotaxic Instrument
Device Class
Class II
Regulation Number
882.4560
Review Panel
NE
Submission Type