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

NEUROVIEW COAXIAL BIPOLAR ELECTRODE

K Number: K955467 · Decision Dec 18, 1995
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
23
Review Days
18

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Basic Information

Device Name
NEUROVIEW COAXIAL BIPOLAR ELECTRODE
K Number
K955467
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Neuro Navigational Corp.
Date Received
November 30, 1995
Decision Date
December 18, 1995
Product Code
GEI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

Similar 510(k) Clearances

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Other Clearances by Neuro Navigational Corp.

K Number Device Name
K965078 2.1MM SEMI-RIGID NEUROVIEW SCISSORS/2.0OMM SEMI-RIGID NEUROVIEW GRASPING FORCEPS
K961406 NEUROVIEW SCISSORS
K961173 1.2MM REUSABLE NEUROVIEW ENDOSCOPE
K961300 ASPIRATION/IRRIGATION CATHETER
K960792 DISPOSABLE NEUROVIEW INTRODUCER SHEATH
K954938 DISPOSABLE NEUROVIEW OPERATING SHEATH
K955351 NEUROVIEW COAXIAL BIPOLAR ELECTRODE
K954899 RIGID NEUROVIEW ENDOSCOPE
K955037 RIGID NEUROVIEW ENDOSCOPE
K952639 DISPOSABLE TOOTHED GRASPING FORCEP
Search all 23 clearances from Neuro Navigational Corp. →