FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

LARYNGEAL SPATULAS

K Number: K822259 · Decision Oct 22, 1982
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
48
Applicant Total
94
Review Days
85

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Basic Information

Device Name
LARYNGEAL SPATULAS
K Number
K822259
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.4350
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
Kelleher Corp.
Date Received
July 29, 1982
Decision Date
October 22, 1982
Product Code
EQH
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

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

Product Code Device Name
EQH Source, Carrier, Fiberoptic Light

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Other Clearances by Kelleher Corp.

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
K822004 FACE SHIELDS
K822185 LARYNGEAL SYRINGE
Search all 94 clearances from Kelleher Corp. →