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ACU-RAY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931279
510(k) Type
Traditional
Applicant
STERNE EQUIPMENT CO., LTD.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
11/3/1993
Days to Decision
240 days
Submission Type
Statement

ACU-RAY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931279
510(k) Type
Traditional
Applicant
STERNE EQUIPMENT CO., LTD.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
11/3/1993
Days to Decision
240 days
Submission Type
Statement