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

DISPOSABLE NEUROVIEW OPERATING SHEATH

K Number: K954938 · Decision Mar 7, 1996
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
90
Applicant Total
23
Review Days
129

Basic Information

Device Name
DISPOSABLE NEUROVIEW OPERATING SHEATH
K Number
K954938
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1480
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
NEURO NAVIGATIONAL CORP.
Date Received
October 30, 1995
Decision Date
March 7, 1996
Product Code
GWG
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
GWG Endoscope, Neurological

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GWG), ordered by most recent decision date.

View all

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
K961300 ASPIRATION/IRRIGATION CATHETER
K961173 1.2MM REUSABLE NEUROVIEW ENDOSCOPE
K960792 DISPOSABLE NEUROVIEW INTRODUCER SHEATH
K955351 NEUROVIEW COAXIAL BIPOLAR ELECTRODE
K954899 RIGID NEUROVIEW ENDOSCOPE
K955467 NEUROVIEW COAXIAL BIPOLAR ELECTRODE
K955037 RIGID NEUROVIEW ENDOSCOPE
K952630 DISPOSABLE BIOPSY FORCEP
Search all 23 clearances from NEURO NAVIGATIONAL CORP. →