FDA 510(k) Applications Submitted by REPRO-MED SYSTEMS, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K102512 | 09/01/2010 | RMS SUBCUTANEOUS NEEDLE SET | REPRO-MED SYSTEMS, INC. |
| K981506 | 04/27/1998 | RESTORE VACUUM ERECTION DEVICE, CONFIDE VACUUM ERECTION DEVICE, PEP (PENILE ERECTION PROGRAM), RELY VACUUM ERECTION DEV) | REPRO-MED SYSTEMS, INC. |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact