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S52D DIGITAL VIDEO LAPAROSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000423
510(k) Type
Traditional
Applicant
SOPRO
Country
France
FDA Decision
Substantially Equivalent
Decision Date
3/31/2000
Days to Decision
51 days
Submission Type
Summary