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VIBRATRON II, VIBRATION SENSITIVITY TESTER

Page Type
Cleared 510(K)
510(k) Number
K863607
510(k) Type
Traditional
Applicant
SENSORTEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/1986
Days to Decision
78 days

VIBRATRON II, VIBRATION SENSITIVITY TESTER

Page Type
Cleared 510(K)
510(k) Number
K863607
510(k) Type
Traditional
Applicant
SENSORTEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/1986
Days to Decision
78 days