The following data is part of a premarket notification filed by Datex-ohmeda with the FDA for Datex-ohmeda Hmef 750.
| Device ID | K031653 |
| 510k Number | K031653 |
| Device Name: | DATEX-OHMEDA HMEF 750 |
| Classification | Filter, Bacterial, Breathing-circuit |
| Applicant | DATEX-OHMEDA 86 PILGRIM RD. Needham, MA 02492 |
| Contact | Joel C Kent |
| Correspondent | Joel C Kent DATEX-OHMEDA 86 PILGRIM RD. Needham, MA 02492 |
| Product Code | CAH |
| CFR Regulation Number | 868.5260 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-05-28 |
| Decision Date | 2003-06-20 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 50190752140088 | K031653 | 000 |
| 20889483602796 | K031653 | 000 |
| 20889483602826 | K031653 | 000 |
| 20889483603175 | K031653 | 000 |
| 20889483601515 | K031653 | 000 |
| 20889483601577 | K031653 | 000 |
| 20889483602536 | K031653 | 000 |
| 20889483602864 | K031653 | 000 |
| 20889483603571 | K031653 | 000 |
| 20190752139104 | K031653 | 000 |
| 20889483601522 | K031653 | 000 |