Last synced on 26 May 2023 at 11:04 pm

AMIA AUTOMATED PD SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K124018
510(k) Type
Traditional
Applicant
DEKA RESEARCH & DEVELOPMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/14/2013
Days to Decision
169 days
Submission Type
Summary

AMIA AUTOMATED PD SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K124018
510(k) Type
Traditional
Applicant
DEKA RESEARCH & DEVELOPMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/14/2013
Days to Decision
169 days
Submission Type
Summary