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VACUUM ERECTION DEVICE (VED)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901223
510(k) Type
Traditional
Applicant
MISSION PHARMACAL CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/1990
Days to Decision
51 days

VACUUM ERECTION DEVICE (VED)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901223
510(k) Type
Traditional
Applicant
MISSION PHARMACAL CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/1990
Days to Decision
51 days