Last synced on 16 August 2024 at 11:05 pm

GIPHY MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883960
510(k) Type
Traditional
Applicant
VASCULAR TECHNOLOGY INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/1989
Days to Decision
379 days

GIPHY MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883960
510(k) Type
Traditional
Applicant
VASCULAR TECHNOLOGY INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/1989
Days to Decision
379 days