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CM 3910 ROTATING DOUBLE SCHEIMPFLUG CAMERA

Page Type
Cleared 510(K)
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)
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