Last synced on 25 April 2025 at 11:05 pm

DIAMOND ND:YAG OPHTHALMIC LASER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901636
510(k) Type
Traditional
Applicant
BIOVISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/1990
Days to Decision
74 days

DIAMOND ND:YAG OPHTHALMIC LASER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901636
510(k) Type
Traditional
Applicant
BIOVISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/1990
Days to Decision
74 days