The following data is part of a premarket notification filed by Electro-cap Intl., Inc. with the FDA for Electro-cap System.
| Device ID | K112319 |
| 510k Number | K112319 |
| Device Name: | ELECTRO-CAP SYSTEM |
| Classification | Electrode, Cutaneous |
| Applicant | ELECTRO-CAP INTL., INC. 1011 WEST LEXINGTON RD. Eaton, OH 45320 |
| Contact | Amy B Swallows |
| Correspondent | Amy B Swallows ELECTRO-CAP INTL., INC. 1011 WEST LEXINGTON RD. Eaton, OH 45320 |
| Product Code | GXY |
| CFR Regulation Number | 882.1320 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-08-11 |
| Decision Date | 2012-01-27 |
| Summary: | summary |