The following data is part of a premarket notification filed by Panasonic Co. Div. Matsu Elec. Corp. America with the FDA for Panasonic Model Ew-213.
| Device ID | K831151 |
| 510k Number | K831151 |
| Device Name: | PANASONIC MODEL EW-213 |
| Classification | System, Measurement, Blood-pressure, Non-invasive |
| Applicant | PANASONIC CO. DIV. MATSU ELEC. CORP. AMERICA 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DXN |
| CFR Regulation Number | 870.1130 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-04-08 |
| Decision Date | 1983-08-11 |