Last synced on 24 May 2024 at 11:04 pm

HELIOBOND

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K802681
510(k) Type
Traditional
Applicant
VIVADENT (USA), INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/24/1980
Days to Decision
27 days

HELIOBOND

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K802681
510(k) Type
Traditional
Applicant
VIVADENT (USA), INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/24/1980
Days to Decision
27 days