FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

CX250 MOBILE GAMMA CAMERA & DCS CONSOLE

K Number: K880878 · Decision Sep 1, 1988
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
129
Applicant Total
181
Review Days
184

Basic Information

Device Name
CX250 MOBILE GAMMA CAMERA & DCS CONSOLE
K Number
K880878
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1100
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
PHILIPS MEDICAL SYSTEMS(CLEVELAND), INC.
Date Received
March 1, 1988
Decision Date
September 1, 1988
Product Code
IYX
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
IYX Camera, Scintillation (Gamma)

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