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INTRAOPERATIVE RADIATION THERAPY DEVICES

Page Type
Cleared 510(K)
510(k) Number
K891261
510(k) Type
Traditional
Applicant
GENERAL ELECTRIC CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/1989
Days to Decision
49 days

INTRAOPERATIVE RADIATION THERAPY DEVICES

Page Type
Cleared 510(K)
510(k) Number
K891261
510(k) Type
Traditional
Applicant
GENERAL ELECTRIC CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/1989
Days to Decision
49 days