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

EAR CANNULAS

K Number: K822201 · Decision Oct 6, 1982
Classifications
1
FEI Numbers
82
Registration Numbers
82
Same Product Code
1
Applicant Total
94
Review Days
75

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Basic Information

Device Name
EAR CANNULAS
K Number
K822201
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Kelleher Corp.
Date Received
July 23, 1982
Decision Date
October 6, 1982
Product Code
FGY
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
FGY Cannula, Injection

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K Number Device Name
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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. →