The following data is part of a premarket notification filed by Johnson & Johnson Medical, Inc. with the FDA for Vaginal Continence Device.
| Device ID | K930618 |
| 510k Number | K930618 |
| Device Name: | VAGINAL CONTINENCE DEVICE |
| Classification | Pessary, Vaginal |
| Applicant | JOHNSON & JOHNSON MEDICAL, INC. P.O. BOX 90130 Arlington, TX 76004 -3130 |
| Contact | Ralph H Larsen |
| Correspondent | Ralph H Larsen JOHNSON & JOHNSON MEDICAL, INC. P.O. BOX 90130 Arlington, TX 76004 -3130 |
| Product Code | HHW |
| CFR Regulation Number | 884.3575 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-02-08 |
| Decision Date | 1995-05-04 |