Company ยท US
Medical Electronic Devices, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1976 to 2005. Name variants (Inc, Corp, punctuation) are merged.
7510(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 |
|---|---|---|---|
| Oct 24, 2005 | K052563 | INOGEN SATELLITE CONSERVER, MODEL SC-100 Medical Electronic Devices, Inc. | NFB |
| May 13, 2004 | K033197 | INOGEN SATELLITE CONSERVER Medical Electronic Devices, Inc. | NFB |
| Oct 25, 2002 | K023420 | PULSED OXYGEN CONSERVING DEVICE - EVERY BREATH, POCDEB, REACTEB Medical Electronic Devices, Inc. | NFB |
| Dec 15, 1998 | K983601 | DEMAND OXYGEN CONSERVING DEVICE, DOCD, THE DOC Medical Electronic Devices, Inc. | NFB |
| Dec 8, 1998 | K983459 | PULSED OXYGEN CONSERVING DEVICE, POCD Medical Electronic Devices, Inc. | NFB |
| Feb 1, 1977 | K770115 | ARTERIAL DIAGNOSTIC UNIT (ADU) Medical Electronic Devices, Inc. | DPW |
| Dec 16, 1976 | K761092 | INGUINAL COMPRESSIVE DEVICE (ICD) Medical Electronic Devices, Inc. |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||