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

MAESTRO DIGITAL IMAGE AND PATIENT RECORD STORAGE SYSTEM

K Number: K970964 · Decision Jun 13, 1997
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
19
Review Days
88

Basic Information

Device Name
MAESTRO DIGITAL IMAGE AND PATIENT RECORD STORAGE SYSTEM
K Number
K970964
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
INTERNATIONAL IMAGING ELECTRONICS
Date Received
March 17, 1997
Decision Date
June 13, 1997
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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