Medical Electronic Devices, Inc.
Medical Electronic Devices, Inc. appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 24, 2005.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K052563 | INOGEN SATELLITE CONSERVER, MODEL SC-100 | October 24, 2005 |
| K033197 | INOGEN SATELLITE CONSERVER | May 13, 2004 |
| K023420 | PULSED OXYGEN CONSERVING DEVICE - EVERY BREATH, POCDEB, REACTEB | October 25, 2002 |
| K983601 | DEMAND OXYGEN CONSERVING DEVICE, DOCD, THE DOC | December 15, 1998 |
| K983459 | PULSED OXYGEN CONSERVING DEVICE, POCD | December 8, 1998 |
| K770115 | ARTERIAL DIAGNOSTIC UNIT (ADU) | February 1, 1977 |
| K761092 | INGUINAL COMPRESSIVE DEVICE (ICD) | December 16, 1976 |