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ZEISS ENDOLIVE STERO ENDOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K950985
510(k) Type
Traditional
Applicant
CARL ZEISS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/1995
Days to Decision
26 days
Submission Type
Summary

ZEISS ENDOLIVE STERO ENDOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K950985
510(k) Type
Traditional
Applicant
CARL ZEISS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/1995
Days to Decision
26 days
Submission Type
Summary