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SELDIX 325 TWO PULSE GENERATOR/CONTROL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883154
510(k) Type
Traditional
Applicant
BAY X-RAY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/1988
Days to Decision
42 days

SELDIX 325 TWO PULSE GENERATOR/CONTROL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883154
510(k) Type
Traditional
Applicant
BAY X-RAY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/1988
Days to Decision
42 days