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MODEL 35300 TRACKER(TM) THERAPY BEAM EVALUATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K874893
510(k) Type
Traditional
Applicant
KEITHLEY INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/17/1988
Days to Decision
78 days

MODEL 35300 TRACKER(TM) THERAPY BEAM EVALUATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K874893
510(k) Type
Traditional
Applicant
KEITHLEY INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/17/1988
Days to Decision
78 days