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VIBRATRON II, VIBRATION SENSITIVITY TESTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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