The following data is part of a premarket notification filed by Draeger Medical, Inc. with the FDA for Spiromed 2.
| Device ID | K851620 |
| 510k Number | K851620 |
| Device Name: | SPIROMED 2 |
| Classification | Spirometer, Diagnostic |
| Applicant | DRAEGER MEDICAL, INC. 148 B. QUARRY RD. Telford, PA 18969 |
| Contact | Edward T Griffith |
| Correspondent | Edward T Griffith DRAEGER MEDICAL, INC. 148 B. QUARRY RD. Telford, PA 18969 |
| Product Code | BZG |
| CFR Regulation Number | 868.1840 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-04-18 |
| Decision Date | 1985-05-10 |