Last synced on 4 February 2023 at 10:33 pm

VISIONARY 2000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000639
510(k) Type
Traditional
Applicant
BURTON MEDICAL PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/25/2000
Days to Decision
90 days
Submission Type
Statement

VISIONARY 2000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000639
510(k) Type
Traditional
Applicant
BURTON MEDICAL PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/25/2000
Days to Decision
90 days
Submission Type
Statement