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VISULINK 900 ARGON

Page Type
Cleared 510(K)
510(k) Number
K952894
510(k) Type
Traditional
Applicant
CARL ZEISS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/1995
Days to Decision
52 days
Submission Type
Summary

VISULINK 900 ARGON

Page Type
Cleared 510(K)
510(k) Number
K952894
510(k) Type
Traditional
Applicant
CARL ZEISS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/1995
Days to Decision
52 days
Submission Type
Summary