The following data is part of a premarket notification filed by Ela Medical, Inc. with the FDA for Unilith 3 Models 7580/7583/7680/7683.
| Device ID | K883037 |
| 510k Number | K883037 |
| Device Name: | UNILITH 3 MODELS 7580/7583/7680/7683 |
| Classification | Implantable Pacemaker Pulse-generator |
| Applicant | ELA MEDICAL, INC. 15245 MINNETONKA BLVD. Minnetonka, MN 55345 |
| Contact | Tom S Anderson |
| Correspondent | Tom S Anderson ELA MEDICAL, INC. 15245 MINNETONKA BLVD. Minnetonka, MN 55345 |
| Product Code | DXY |
| CFR Regulation Number | 870.3610 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-07-19 |
| Decision Date | 1989-01-25 |