Company ยท US
Elekon Industries U.S.A., Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2004 to 2004. 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 |
|---|---|---|---|
| Dec 29, 2004 | K042705 | DISPOSABLE NON-ADHESIVE SPO2 SENSORS Elekon Industries U.S.A., Inc. | DQA |
| Dec 6, 2004 | K042675 | FLEXI-STAT SP02 EAR SENSOR Elekon Industries U.S.A., Inc. | DPZ |
| Nov 26, 2004 | K042704 | REUSABLE FINGER CLIP SPO2 SENSORS Elekon Industries U.S.A., Inc. | DQA |
| Sep 14, 2004 | K041522 | FLEXI-STAT DISPOSABLE ADHESIVE SPO2 SENSORS Elekon Industries U.S.A., Inc. | DQA |
| Sep 2, 2004 | K041647 | FLEXI-STAT REUSABLE FINGER CLIP SPO2 SENSORS (NELLCOR-COMPATIBLE),(BCI-COMPATIBLE), (DATEX-COMPATIBLE) Elekon Industries U.S.A., Inc. | DQA |
| Jul 29, 2004 | K041644 | FLEXI-STAT DISPOSABLE NON-ADHESIVE SPO2 SENSORS, (NELLCOR-COMPATIBLE), (BCI-COMPATIBLE), (DATEX-COMPATIBLE) Elekon Industries U.S.A., Inc. | DQA |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||