Last synced on 25 April 2025 at 11:05 pm

DDS, DS3000, RS3000, CS5000, OT3000, IS3000, RS5000, CD3000, US3000, (AMONGST OTHER NAMES)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993532
510(k) Type
Traditional
Applicant
IMPAX TECHNOLOGY, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
12/15/1999
Days to Decision
57 days
Submission Type
Summary

DDS, DS3000, RS3000, CS5000, OT3000, IS3000, RS5000, CD3000, US3000, (AMONGST OTHER NAMES)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993532
510(k) Type
Traditional
Applicant
IMPAX TECHNOLOGY, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
12/15/1999
Days to Decision
57 days
Submission Type
Summary