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AESPIRE 7900, AESPIRE VIEW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092864
510(k) Type
Special
Applicant
Datex-Ohmeda Inc., A Division of Instrumentarium C
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2010
Days to Decision
117 days
Submission Type
Summary

AESPIRE 7900, AESPIRE VIEW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092864
510(k) Type
Special
Applicant
Datex-Ohmeda Inc., A Division of Instrumentarium C
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2010
Days to Decision
117 days
Submission Type
Summary