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

JACKSON BITE BLOCKS

K Number: K822018 · Decision Aug 3, 1982
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
27
Applicant Total
94
Review Days
26

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Basic Information

Device Name
JACKSON BITE BLOCKS
K Number
K822018
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5070
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Kelleher Corp.
Date Received
July 8, 1982
Decision Date
August 3, 1982
Product Code
JXL
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
JXL Block, Bite

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K Number Device Name
K822268 NAGASHIMA NS-III ELECTRONYSTAGMOGRAPH
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
Search all 94 clearances from Kelleher Corp. →