Last synced on 16 May 2025 at 11:05 pm

RIGHT ATRIAL CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K930630
510(k) Type
Traditional
Applicant
AKCESS MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
2/7/1994
Days to Decision
364 days
Submission Type
Statement

RIGHT ATRIAL CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K930630
510(k) Type
Traditional
Applicant
AKCESS MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
2/7/1994
Days to Decision
364 days
Submission Type
Statement