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

NAGASHIMA NS-III ELECTRONYSTAGMOGRAPH

K Number: K822268 · Decision Jan 28, 1983
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
58
Applicant Total
94
Review Days
183

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Basic Information

Device Name
NAGASHIMA NS-III ELECTRONYSTAGMOGRAPH
K Number
K822268
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1460
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Kelleher Corp.
Date Received
July 29, 1982
Decision Date
January 28, 1983
Product Code
GWN
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
GWN Nystagmograph

Similar 510(k) Clearances

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Other Clearances by Kelleher Corp.

K Number Device Name
K822618 EMERGENCY TRACHEOSTOMY INSTRUMENT SET
K823083 ELECTROSURGICAL UNIT
K823111 NYSTYMOGRAPH ACCESS
K822252 ENT TREATMENT UNITS
K822272 HEAD MIRRORS W/HEAD LAMPS & HEAD BANDS
K822017 TYMPANOSTOMY TUBES & VARIOUS TYPES
K822257 VARIOUS TYPES OF LIGHT SOURCE HANDLES
K822259 LARYNGEAL SPATULAS
K822004 FACE SHIELDS
K822185 LARYNGEAL SYRINGE
Search all 94 clearances from Kelleher Corp. →