Last synced on 23 September 2022 at 11:05 pm

SMARTLYTE ELECTROLYTE ANALYZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121040
510(k) Type
Traditional
Applicant
DIAMOND DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/2012
Days to Decision
147 days
Submission Type
Summary

SMARTLYTE ELECTROLYTE ANALYZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121040
510(k) Type
Traditional
Applicant
DIAMOND DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/2012
Days to Decision
147 days
Submission Type
Summary