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

ENT FORCEPS

K Number: K822278 · Decision Aug 27, 1982
Classifications
1
FEI Numbers
444
Registration Numbers
445
Same Product Code
103
Applicant Total
94
Review Days
29

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Basic Information

Device Name
ENT FORCEPS
K Number
K822278
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Kelleher Corp.
Date Received
July 29, 1982
Decision Date
August 27, 1982
Product Code
GEN
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
GEN Forceps, General & Plastic Surgery

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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
K822259 LARYNGEAL SPATULAS
K822004 FACE SHIELDS
Search all 94 clearances from Kelleher Corp. →