The following data is part of a premarket notification filed by Fisher Scientific Co., Llc. with the FDA for Flush Solution Concentrate.
| Device ID | K831020 |
| 510k Number | K831020 |
| Device Name: | FLUSH SOLUTION CONCENTRATE |
| Classification | Electrode Measurement, Blood-gases (pco2, Po2) And Blood Ph |
| Applicant | FISHER SCIENTIFIC CO., LLC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CHL |
| CFR Regulation Number | 862.1120 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-03-30 |
| Decision Date | 1983-05-09 |