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ZEISS LASER INDIRECT OPHTHALMOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K924588
510(k) Type
Traditional
Applicant
CARL ZEISS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/1993
Days to Decision
302 days
Submission Type
Statement

ZEISS LASER INDIRECT OPHTHALMOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K924588
510(k) Type
Traditional
Applicant
CARL ZEISS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/1993
Days to Decision
302 days
Submission Type
Statement