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

SPECIMEN COLLECTORS

K Number: K822005 · Decision Jul 28, 1982
Classifications
1
FEI Numbers
193
Registration Numbers
193
Same Product Code
86
Applicant Total
94
Review Days
20

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Basic Information

Device Name
SPECIMEN COLLECTORS
K Number
K822005
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Kelleher Corp.
Date Received
July 8, 1982
Decision Date
July 28, 1982
Product Code
GCX
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
GCX Apparatus, Suction, Operating-Room, Wall Vacuum Powered

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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. →