The following data is part of a premarket notification filed by Siemens Medical Electronics with the FDA for Siemens Micro2 Pulse Oximeter.
| Device ID | K913489 |
| 510k Number | K913489 |
| Device Name: | SIEMENS MICRO2 PULSE OXIMETER |
| Classification | Oximeter |
| Applicant | SIEMENS MEDICAL ELECTRONICS 16 ELECTRONICS AVE. Danvers, MA 01923 |
| Contact | Robert R Murfitt |
| Correspondent | Robert R Murfitt SIEMENS MEDICAL ELECTRONICS 16 ELECTRONICS AVE. Danvers, MA 01923 |
| Product Code | DQA |
| CFR Regulation Number | 870.2700 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-08-06 |
| Decision Date | 1991-10-30 |