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 |