Last synced on 30 September 2022 at 11:05 pm

REDON SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001716
510(k) Type
Traditional
Applicant
PFM PRODUKTE FUR DIE MEDIZIN AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2000
Days to Decision
44 days
Submission Type
Summary

REDON SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001716
510(k) Type
Traditional
Applicant
PFM PRODUKTE FUR DIE MEDIZIN AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2000
Days to Decision
44 days
Submission Type
Summary