The following data is part of a premarket notification filed by Transidyne General Corp. with the FDA for Corometrics Medical Systems 220 Ph Sys..
| Device ID | K800271 |
| 510k Number | K800271 |
| Device Name: | COROMETRICS MEDICAL SYSTEMS 220 PH SYS. |
| Classification | Electrode Measurement, Blood-gases (pco2, Po2) And Blood Ph |
| Applicant | TRANSIDYNE GENERAL CORP. 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 | 1980-02-06 |
| Decision Date | 1980-02-26 |