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510(k) K112094

BRAIN BIOPSY NEEDLE by Ad-Tech Medical Instrument Corp — Product Code HAW

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 24, 2012
Date Received
July 22, 2011
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

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  • K970587 — AD-TECH SUBDURAL ELECTRODE (May 9, 1997)
  • K964644 — AD-TECH'S DEPTH ELECTRODE (May 9, 1997)
  • K940320 — AD-TECH'S RAAB INFANT NASOPHARYNGEAL PRONGS (September 19, 1995)
  • K944061 — CUEVA CRANIAL NERVE ELECTRODE (January 20, 1995)

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