The following data is part of a premarket notification filed by Ela Medical, Inc. with the FDA for Pacing System Analyzer Psa Sce-22.
| Device ID | K791975 |
| 510k Number | K791975 |
| Device Name: | PACING SYSTEM ANALYZER PSA SCE-22 |
| Classification | Analyzer, Pacemaker Generator Function |
| Applicant | ELA MEDICAL, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DTC |
| CFR Regulation Number | 870.3630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-10-02 |
| Decision Date | 1980-01-31 |