The following data is part of a premarket notification filed by Autovage with the FDA for Quicvage.
| Device ID | K914907 |
| 510k Number | K914907 |
| Device Name: | QUICVAGE |
| Classification | Catheter (gastric, Colonic, Etc.), Irrigation And Aspiration |
| Applicant | AUTOVAGE 1631 CITATION DR. South Park, PA 15129 |
| Contact | Joseph P Rudolph |
| Correspondent | Joseph P Rudolph AUTOVAGE 1631 CITATION DR. South Park, PA 15129 |
| Product Code | KDH |
| CFR Regulation Number | 876.5980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-11-01 |
| Decision Date | 1992-01-24 |