Last synced on 27 January 2023 at 11:04 pm

DENVER PLEURX PLEURAL CATHETER KIT, CATALOG NO. 50-7000, DENVER PLEURX HOME DRAINAGE KIT, CATALOG NO. 50-7500

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971753
510(k) Type
Traditional
Applicant
DENVER BIOMATERIALS, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
6/27/1997
Days to Decision
46 days
Submission Type
Summary

DENVER PLEURX PLEURAL CATHETER KIT, CATALOG NO. 50-7000, DENVER PLEURX HOME DRAINAGE KIT, CATALOG NO. 50-7500

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971753
510(k) Type
Traditional
Applicant
DENVER BIOMATERIALS, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
6/27/1997
Days to Decision
46 days
Submission Type
Summary