Last synced on 30 September 2022 at 11:05 pm

IONOMETER EH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901039
510(k) Type
Traditional
Applicant
FRESENIUS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/1990
Days to Decision
114 days

IONOMETER EH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901039
510(k) Type
Traditional
Applicant
FRESENIUS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/1990
Days to Decision
114 days