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

HALL CANNLULA SYSTEM

K Number: K862778 · Decision Sep 8, 1986
Classifications
1
FEI Numbers
386
Registration Numbers
386
Same Product Code
680
Applicant Total
8
Review Days
48

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Basic Information

Device Name
HALL CANNLULA SYSTEM
K Number
K862778
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Hall Surgical, Division of Zimmer, Inc.
Date Received
July 22, 1986
Decision Date
September 8, 1986
Product Code
HRX
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
HRX Arthroscope

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Other Clearances by Hall Surgical, Division of Zimmer, Inc.

K Number Device Name
K942660 HALL MICROCHOICE ELECTRIC POWERED SYSTEM
K864734 HALL ORAL IMPLANT SYSTEM
K864929 HALL (R) MICRO E POWERED SURGICAL INSTRUMENT SYST
K864163 HALL DUNBAR DRILL GUIDE SYSTEM
K862474 HALL STERNUM SAW
K862529 HALL STERILE BUR
K852143 HALL IRRIGATION SYSTEM