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

CESIUM-137 AFTERLOADING SYSTEM /GYN.BRA.

K Number: K800320 · Decision Mar 25, 1980
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
35
Applicant Total
94
Review Days
42

Basic Information

Device Name
CESIUM-137 AFTERLOADING SYSTEM /GYN.BRA.
K Number
K800320
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.5650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
AMERSHAM CORP.
Date Received
February 12, 1980
Decision Date
March 25, 1980
Product Code
IWJ
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
IWJ System, Applicator, Radionuclide, Manual

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