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

REGISTREX 1000 DIGITAL RADIOGRAPHY SYS

K Number: K833230 · Decision Nov 21, 1983
Classifications
1
FEI Numbers
139
Registration Numbers
139
Same Product Code
297
Applicant Total
61
Review Days
89

Basic Information

Device Name
REGISTREX 1000 DIGITAL RADIOGRAPHY SYS
K Number
K833230
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
ADVANCED TECHNOLOGY LABORATORIES, INC.
Date Received
August 24, 1983
Decision Date
November 21, 1983
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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