Last synced on 24 June 2022 at 11:05 pm

Aestiva 7900, Aestiva MRI, Aestiva 7100, Aestiva 7100 Compact, Aespire 100, Aespire 7100, Aespire 7900, Aespire View, Avance, Avance CS2, Aisys, Aisys CS2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172045
510(k) Type
Traditional
Applicant
Datex-Ohmeda, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/2017
Days to Decision
120 days
Submission Type
Summary

Aestiva 7900, Aestiva MRI, Aestiva 7100, Aestiva 7100 Compact, Aespire 100, Aespire 7100, Aespire 7900, Aespire View, Avance, Avance CS2, Aisys, Aisys CS2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172045
510(k) Type
Traditional
Applicant
Datex-Ohmeda, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/2017
Days to Decision
120 days
Submission Type
Summary