Last synced on 23 September 2022 at 11:05 pm

PROXENON 350, MODEL 902XX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071218
510(k) Type
Traditional
Applicant
WELCH ALLYN, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/14/2007
Days to Decision
43 days
Submission Type
Summary

PROXENON 350, MODEL 902XX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071218
510(k) Type
Traditional
Applicant
WELCH ALLYN, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/14/2007
Days to Decision
43 days
Submission Type
Summary