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RESTORE VACUUM ERECTION DEVICE, CONFIDE VACUUM ERECTION DEVICE, PEP (PENILE ERECTION PROGRAM), RELY VACUUM ERECTION DEV)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981506
510(k) Type
Traditional
Applicant
REPRO-MED SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/25/1998
Days to Decision
59 days
Submission Type
Summary

RESTORE VACUUM ERECTION DEVICE, CONFIDE VACUUM ERECTION DEVICE, PEP (PENILE ERECTION PROGRAM), RELY VACUUM ERECTION DEV)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981506
510(k) Type
Traditional
Applicant
REPRO-MED SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/25/1998
Days to Decision
59 days
Submission Type
Summary