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CM 3910 ROTATING DOUBLE SCHEIMPFLUG CAMERA

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051940
510(k) Type
Traditional
Applicant
Sis Ltd., Surgical Instrument Systems
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/2005
Days to Decision
72 days
Submission Type
Summary

CM 3910 ROTATING DOUBLE SCHEIMPFLUG CAMERA

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051940
510(k) Type
Traditional
Applicant
Sis Ltd., Surgical Instrument Systems
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/2005
Days to Decision
72 days
Submission Type
Summary