FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MICROTARGETING STAR DRIVE SYSTEM, COMPONENTS

K Number: K092562 · Decision Sep 18, 2009
Classifications
1
FEI Numbers
250
Registration Numbers
250
Same Product Code
422
Applicant Total
12
Review Days
29

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Basic Information

Device Name
MICROTARGETING STAR DRIVE SYSTEM, COMPONENTS
K Number
K092562
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
FHC, Inc.
Date Received
August 20, 2009
Decision Date
September 18, 2009
Product Code
HAW
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HAW Neurological Stereotaxic Instrument

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Other Clearances by FHC, Inc.

K Number Device Name
K231141 STarFix Designer Software C0265
K200169 VFS1 Bipolar Electrosurgical Generator
K183123 microTargeting Guideline 4000 5.0 System
K121950 MICROTARGETING XL STAR DRIVE SYSTEM
K092192 WAYPOINT STEREOTACTIC SYSTEM
K071364 MICROTARGETING GUIDELINE 4000
K033173 MICRO TARGETING ELECTRODE
K011775 MICRO TARGETING DRIVE SYSTEM
K011992 FHC MICROTARGETING DRIVE SYSTEM
K003776 MICROTARGETING DRIVE SYSTEM
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