Last synced on 21 June 2024 at 11:04 pm

ARTERIAL ANCHOR BANDAGE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883957
510(k) Type
Traditional
Applicant
GUIDELINES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/1988
Days to Decision
29 days

ARTERIAL ANCHOR BANDAGE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883957
510(k) Type
Traditional
Applicant
GUIDELINES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/1988
Days to Decision
29 days