Last synced on 6 December 2024 at 11:05 pm

ELASTOPLAST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K831438
510(k) Type
Traditional
Applicant
BEIERSDORF, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/1983
Days to Decision
204 days

ELASTOPLAST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K831438
510(k) Type
Traditional
Applicant
BEIERSDORF, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/1983
Days to Decision
204 days