Company ยท US
The Electrode Store, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1995 to 2009. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 14, 2009 | K083758 | SENSORY NERVE ELECTRODES-TWO FINGER RINGS, STIMULATOR PROBE ELECTRODES-FACIAL, MONO, BI- & TRIPOLAR NERVE STIMULATORS The Electrode Store, Inc. | GXY |
| Aug 13, 2002 | K022197 | SURFACE ELECTRODE FOR ELECTROENCEPHALOGRAPHY The Electrode Store, Inc. | GXY |
| Jul 19, 2002 | K020910 | SUBDERMAL NEEDLE ELECTRODE FOR ELECTROENCEPHALOGRAPHY, MODELS PRO-E12SAF AND DEN-12SAF The Electrode Store, Inc. | GXZ |
| May 10, 2002 | K020445 | THE ELECTRODE STORE SURFACE (CUTANEOUS) ELECTRODE FOR EMG The Electrode Store, Inc. | GXY |
| Dec 6, 1995 | K926094 | PROTECTRODE SYSTEM The Electrode Store, Inc. | GXZ |
| Nov 16, 1995 | K932691 | PROTECTRODE SYSTEMS CONCENTRIC The Electrode Store, Inc. | IKT |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||