Last synced on 27 January 2023 at 11:04 pm

GRIND GUARD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090472
510(k) Type
Traditional
Applicant
ARCHTEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/14/2009
Days to Decision
232 days
Submission Type
Summary

GRIND GUARD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090472
510(k) Type
Traditional
Applicant
ARCHTEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/14/2009
Days to Decision
232 days
Submission Type
Summary