The following data is part of a premarket notification filed by Resound Corp. with the FDA for Resound Impression Material.
| Device ID | K892935 |
| 510k Number | K892935 |
| Device Name: | RESOUND IMPRESSION MATERIAL |
| Classification | Material, Impression |
| Applicant | RESOUND CORP. 220 SAGINAW DRIVE, SEAPORT CENTRE Redwood City, CA 94063 |
| Contact | Vincent Pluvinage |
| Correspondent | Vincent Pluvinage RESOUND CORP. 220 SAGINAW DRIVE, SEAPORT CENTRE Redwood City, CA 94063 |
| Product Code | ELW |
| CFR Regulation Number | 872.3660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-04-21 |
| Decision Date | 1989-07-14 |