Last synced on 6 December 2024 at 11:05 pm

POLESTAR N-10

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010850
510(k) Type
Traditional
Applicant
ODIN MEDICAL TECHNOLOGIES LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
12/17/2001
Days to Decision
271 days
Submission Type
Summary