The following data is part of a premarket notification filed by Siemens Elema Ab with the FDA for Patient Tubing Hytrel Siemens-elema.
| Device ID | K841657 |
| 510k Number | K841657 |
| Device Name: | PATIENT TUBING HYTREL SIEMENS-ELEMA |
| Classification | Set, Tubing And Support, Ventilator (w Harness) |
| Applicant | SIEMENS ELEMA AB 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | BZO |
| CFR Regulation Number | 868.5975 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-04-23 |
| Decision Date | 1984-05-23 |