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

FRANKLIN 9000 WALL STAND

K Number: K905789 · Decision May 20, 1991
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
25
Applicant Total
27
Review Days
144

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Basic Information

Device Name
FRANKLIN 9000 WALL STAND
K Number
K905789
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1860
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Mallinckrodt Group, Inc.
Date Received
December 27, 1990
Decision Date
May 20, 1991
Product Code
KPX
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
KPX Changer, Radiographic Film/Cassette

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