Repro-Med Systems, Inc.
6 FDA 510(k) clearances · Manufacturer
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| RMS SUBCUTANEOUS NEEDLE SET (K102512) | Repro-Med Systems, Inc. | 2011-05-20 |
| RESTORE VACUUM ERECTION DEVICE, CONFIDE VACUUM ERECTION DEVICE, PEP (PENILE ERECTION PROGRAM), RELY VACUUM ERECTION DEV) (K981506) | Repro-Med Systems, Inc. | 1998-06-25 |
| FREEDOM 60 SYRINGE INFUSION PUMP SYSTEM WITH SYRINGE SET & TUBING (K933652) | Repro-Med Systems, Inc. | 1994-05-18 |
| REPRO-MED EMERGENCY AIRWAY VACUUM SYSTEM (K894299) | Repro-Med Systems, Inc. | 1989-09-22 |
| REPRO-MED NEONATE ASPIRATION SYSTEM (K892529) | Repro-Med Systems, Inc. | 1989-06-12 |
| REPRO-MED SYSTEMS INFUSION DEVICE (K844401) | Repro-Med Systems, Inc. | 1985-03-12 |
Track Repro-Med Systems, Inc. automatically
Every clearance here is in the API, with alerts when new ones post.