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

DIGITAL FLUOROGRAPHIC IMAGING SYSTEM DIGIFORMER

K Number: K844037 · Decision Mar 1, 1985
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
54
Review Days
136

Basic Information

Device Name
DIGITAL FLUOROGRAPHIC IMAGING SYSTEM DIGIFORMER
K Number
K844037
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
TOSHIBA MEDICAL SYSTEMS
Date Received
October 16, 1984
Decision Date
March 1, 1985
Product Code
LLZ
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
LLZ System, Image Processing, Radiological

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