Last synced on 24 May 2024 at 11:04 pm

RONDOFLEX PLUS 360

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K042872
510(k) Type
Special
Applicant
KAVO AMERICA CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/2004
Days to Decision
36 days
Submission Type
Summary

RONDOFLEX PLUS 360

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K042872
510(k) Type
Special
Applicant
KAVO AMERICA CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/2004
Days to Decision
36 days
Submission Type
Summary