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MODIFICATION TO VISTA STEREOSCOPE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K020301
510(k) Type
Special
Applicant
VISTA MEDICAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/2002
Days to Decision
14 days
Submission Type
Summary

MODIFICATION TO VISTA STEREOSCOPE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K020301
510(k) Type
Special
Applicant
VISTA MEDICAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/2002
Days to Decision
14 days
Submission Type
Summary