The following data is part of a premarket notification filed by Electro-catheter Corp. with the FDA for Silicore Semi-floater.
| Device ID | K934787 |
| 510k Number | K934787 |
| Device Name: | SILICORE SEMI-FLOATER |
| Classification | Electrode, Pacemaker, Temporary |
| Applicant | ELECTRO-CATHETER CORP. 2100 FELVER COURT P.O. BOX 1214C Rahway, NJ 07065 |
| Contact | Lorraine T Montemurro |
| Correspondent | Lorraine T Montemurro ELECTRO-CATHETER CORP. 2100 FELVER COURT P.O. BOX 1214C Rahway, NJ 07065 |
| Product Code | LDF |
| CFR Regulation Number | 870.3680 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-10-05 |
| Decision Date | 1995-02-24 |