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PBN DILATORS

Page Type
Cleared 510(K)
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)
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