The following data is part of a premarket notification filed by Criticare Systems, Inc. with the FDA for 503 Pulse Oximeter.
| Device ID | K911124 |
| 510k Number | K911124 |
| Device Name: | 503 PULSE OXIMETER |
| Classification | Oximeter |
| Applicant | CRITICARE SYSTEMS, INC. P.O. BOX 26556 Milwaukee, WI 53226 |
| Contact | Der Ruhr |
| Correspondent | Der Ruhr CRITICARE SYSTEMS, INC. P.O. BOX 26556 Milwaukee, WI 53226 |
| Product Code | DQA |
| CFR Regulation Number | 870.2700 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-03-12 |
| Decision Date | 1991-06-07 |