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

ELECTROSURGICAL UNIT

K Number: K823083 · Decision Dec 7, 1982
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
94
Review Days
49

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Basic Information

Device Name
ELECTROSURGICAL UNIT
K Number
K823083
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Kelleher Corp.
Date Received
October 19, 1982
Decision Date
December 7, 1982
Product Code
GEI
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
GEI Electrosurgical, Cutting & Coagulation & Accessories

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Other Clearances by Kelleher Corp.

K Number Device Name
K822268 NAGASHIMA NS-III ELECTRONYSTAGMOGRAPH
K822618 EMERGENCY TRACHEOSTOMY INSTRUMENT SET
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. →