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Celeris, Disposable Sinus Debrider

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212650
510(k) Type
Traditional
Applicant
Gyrus ACMI, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2022
Days to Decision
149 days
Submission Type
Summary

Celeris, Disposable Sinus Debrider

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212650
510(k) Type
Traditional
Applicant
Gyrus ACMI, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2022
Days to Decision
149 days
Submission Type
Summary