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

ENT TREATMENT UNITS

K Number: K822252 · Decision Nov 22, 1982
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
31
Applicant Total
94
Review Days
116

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Basic Information

Device Name
ENT TREATMENT UNITS
K Number
K822252
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.5300
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
Kelleher Corp.
Date Received
July 29, 1982
Decision Date
November 22, 1982
Product Code
ETF
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
ETF Unit, Examining/Treatment, Ent

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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
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. →