Last synced on 2 December 2022 at 11:04 pm

PHD PERSONAL HEMODIALYSIS INSTRUMENT-1M101, PHD WATER PRE-TREATMENT KIT-1W605,PHD HARD PLUMBING KIT-1W604, PHD BLOOD TUB

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010131
510(k) Type
Traditional
Applicant
AKSYS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/26/2002
Days to Decision
434 days
Submission Type
Summary

PHD PERSONAL HEMODIALYSIS INSTRUMENT-1M101, PHD WATER PRE-TREATMENT KIT-1W605,PHD HARD PLUMBING KIT-1W604, PHD BLOOD TUB

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010131
510(k) Type
Traditional
Applicant
AKSYS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/26/2002
Days to Decision
434 days
Submission Type
Summary