The following data is part of a premarket notification filed by Ferris Mfg. Corp. with the FDA for Electrodes, Ferris Ecg, Types 905,906.
| Device ID | K790305 |
| 510k Number | K790305 |
| Device Name: | ELECTRODES, FERRIS ECG, TYPES 905,906 |
| Classification | Electrode, Electrocardiograph |
| Applicant | FERRIS MFG. CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DRX |
| CFR Regulation Number | 870.2360 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-02-13 |
| Decision Date | 1979-04-03 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20884838006991 | K790305 | 000 |