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MM-22 MICROTRON

Page Type
Cleared 510(K)
510(k) Number
K827704
510(k) Type
Traditional
Applicant
INSTRUMENT AB SCANDITRONIX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/1982
Days to Decision
90 days

MM-22 MICROTRON

Page Type
Cleared 510(K)
510(k) Number
K827704
510(k) Type
Traditional
Applicant
INSTRUMENT AB SCANDITRONIX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/1982
Days to Decision
90 days