Last synced on 27 March 2026 at 11:12 pm

O-020 LASER INDIRECT OPHTHALMOSCOPE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890787
510(k) Type
Traditional
Applicant
HGM MEDICAL LASER SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1989
Days to Decision
37 days

O-020 LASER INDIRECT OPHTHALMOSCOPE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890787
510(k) Type
Traditional
Applicant
HGM MEDICAL LASER SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1989
Days to Decision
37 days