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ZEISS VISULAS ARGON LASER

Page Type
Cleared 510(K)
510(k) Number
K874609
510(k) Type
Traditional
Applicant
CARL ZEISS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/6/1988
Days to Decision
58 days

ZEISS VISULAS ARGON LASER

Page Type
Cleared 510(K)
510(k) Number
K874609
510(k) Type
Traditional
Applicant
CARL ZEISS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/6/1988
Days to Decision
58 days