The following data is part of a premarket notification filed by Chalgren Enterprises, Inc. with the FDA for Emg Recording Ring Electrode.
| Device ID | K953356 |
| 510k Number | K953356 |
| Device Name: | EMG RECORDING RING ELECTRODE |
| Classification | Electrode, Cutaneous |
| Applicant | CHALGREN ENTERPRISES, INC. 8021 CARMEL ST. SUITE B Gilroy, CA 95020 |
| Contact | Richard Kaiser |
| Correspondent | Richard Kaiser CHALGREN ENTERPRISES, INC. 8021 CARMEL ST. SUITE B Gilroy, CA 95020 |
| Product Code | GXY |
| CFR Regulation Number | 882.1320 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-07-17 |
| Decision Date | 1996-01-22 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00816020020771 | K953356 | 000 |
| 00816020020764 | K953356 | 000 |
| 00816020020757 | K953356 | 000 |
| 00816020020740 | K953356 | 000 |
| 00816020020733 | K953356 | 000 |
| 00816020020726 | K953356 | 000 |
| 00816020020719 | K953356 | 000 |
| 00816020020702 | K953356 | 000 |