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ELIOS DIODE OPHTHALMIC LASER

Page Type
Cleared 510(K)
510(k) Number
K921320
510(k) Type
Traditional
Applicant
MARCO OPHTHALMIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/1992
Days to Decision
105 days
Submission Type
Statement

ELIOS DIODE OPHTHALMIC LASER

Page Type
Cleared 510(K)
510(k) Number
K921320
510(k) Type
Traditional
Applicant
MARCO OPHTHALMIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/1992
Days to Decision
105 days
Submission Type
Statement