The following data is part of a premarket notification filed by Oximetrix, Inc. with the FDA for Pump Infusion Wearable Infusion Pump.
| Device ID | K833966 |
| 510k Number | K833966 |
| Device Name: | PUMP INFUSION WEARABLE INFUSION PUMP |
| Classification | Culture Media, Selective And Non-differential |
| Applicant | OXIMETRIX, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | JSJ |
| CFR Regulation Number | 866.2360 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-11-16 |
| Decision Date | 1984-01-25 |