The following data is part of a premarket notification filed by Currie Medical Specialties, Inc. with the FDA for Abg Kits - Cms 4000 Series.
| Device ID | K830333 |
| 510k Number | K830333 |
| Device Name: | ABG KITS - CMS 4000 SERIES |
| Classification | Arterial Blood Sampling Kit |
| Applicant | CURRIE MEDICAL SPECIALTIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CBT |
| CFR Regulation Number | 868.1100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-02-01 |
| Decision Date | 1983-03-31 |