The following data is part of a premarket notification filed by Medical Marketing Group with the FDA for Mmg Uro-self Catheter.
| Device ID | K871999 |
| 510k Number | K871999 |
| Device Name: | MMG URO-SELF CATHETER |
| Classification | Catheter, Urethral |
| Applicant | MEDICAL MARKETING GROUP 5335 DIVIDEND DR. Decatur, GA 30035 |
| Contact | Timothy D Golden |
| Correspondent | Timothy D Golden MEDICAL MARKETING GROUP 5335 DIVIDEND DR. Decatur, GA 30035 |
| Product Code | GBM |
| CFR Regulation Number | 876.5130 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-05-26 |
| Decision Date | 1987-08-25 |