Last synced on 2 December 2022 at 11:04 pm

DYNAMEQ-II OPTION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K955466
510(k) Type
Traditional
Applicant
QUALITONE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1996
Days to Decision
75 days
Submission Type
Summary