Last synced on 12 July 2024 at 11:04 pm

S51D DIGITAL ENDOSCOPY CAMERA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000424
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