Last synced on 20 December 2024 at 11:05 pm

VERTIGONE BPPV GOGGLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082634
510(k) Type
Traditional
Applicant
VERTIGONE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/2009
Days to Decision
209 days
Submission Type
Summary

VERTIGONE BPPV GOGGLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082634
510(k) Type
Traditional
Applicant
VERTIGONE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/2009
Days to Decision
209 days
Submission Type
Summary