Last synced on 2 December 2022 at 11:04 pm

ULTRX(TM) 850 ARTIFICIAL KIDNEY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884353
510(k) Type
Traditional
Applicant
CD MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/1988
Days to Decision
52 days

ULTRX(TM) 850 ARTIFICIAL KIDNEY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884353
510(k) Type
Traditional
Applicant
CD MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/1988
Days to Decision
52 days