The following data is part of a premarket notification filed by Respironics, Inc. with the FDA for Eocd.
| Device ID | K041568 |
| 510k Number | K041568 |
| Device Name: | EOCD |
| Classification | Conserver, Oxygen |
| Applicant | RESPIRONICS, INC. 1001 MURRY RIDGE LN. Murrysville, PA 15668 |
| Contact | Lou Anne Kinney |
| Correspondent | Lou Anne Kinney RESPIRONICS, INC. 1001 MURRY RIDGE LN. Murrysville, PA 15668 |
| Product Code | NFB |
| CFR Regulation Number | 868.5905 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-06-10 |
| Decision Date | 2004-07-21 |
| Summary: | summary |