Last synced on 6 June 2025 at 11:06 pm

ELIOS DIODE OPHTHALMIC LASER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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