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

ORBITOR

K Number: K800639 · Decision May 14, 1980
Classifications
1
FEI Numbers
139
Registration Numbers
139
Same Product Code
297
Applicant Total
181
Review Days
51

Basic Information

Device Name
ORBITOR
K Number
K800639
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
PHILIPS MEDICAL SYSTEMS(CLEVELAND), INC.
Date Received
March 24, 1980
Decision Date
May 14, 1980
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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