Last synced on 11 July 2025 at 11:06 pm

CORDIPAK CARDIAC CATHETERIZATION PACK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K863337
510(k) Type
Traditional
Applicant
ANGI-PAK CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/1986
Days to Decision
32 days

CORDIPAK CARDIAC CATHETERIZATION PACK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K863337
510(k) Type
Traditional
Applicant
ANGI-PAK CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/1986
Days to Decision
32 days