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

DIGITAL RADIOGRAPHY SYSTEM

K Number: K810364 · Decision Mar 11, 1981
Classifications
1
FEI Numbers
139
Registration Numbers
139
Same Product Code
297
Applicant Total
88
Review Days
27

Basic Information

Device Name
DIGITAL RADIOGRAPHY SYSTEM
K Number
K810364
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
ADAC LABORATORIES
Date Received
February 12, 1981
Decision Date
March 11, 1981
Product Code
JAA
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
JAA System, X-Ray, Fluoroscopic, Image-Intensified

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