Last synced on 2 December 2022 at 11:04 pm

PBN DILATORS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990808
510(k) Type
Traditional
Applicant
MEDICAL DEVICE TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/26/1999
Days to Decision
260 days
Submission Type
Summary

PBN DILATORS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990808
510(k) Type
Traditional
Applicant
MEDICAL DEVICE TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/26/1999
Days to Decision
260 days
Submission Type
Summary