Last synced on 25 April 2025 at 11:05 pm

CATHETER,PERCUTANEOUS INTRODUC. & SHEATH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K770561
510(k) Type
Traditional
Applicant
USCI, DIV. C.R. BARD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/1977
Days to Decision
34 days

CATHETER,PERCUTANEOUS INTRODUC. & SHEATH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K770561
510(k) Type
Traditional
Applicant
USCI, DIV. C.R. BARD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/1977
Days to Decision
34 days