The following data is part of a premarket notification filed by Ppg Industries, Inc. with the FDA for Non-invasive Blood Pressure Module.
| Device ID | K875265 |
| 510k Number | K875265 |
| Device Name: | NON-INVASIVE BLOOD PRESSURE MODULE |
| Classification | System, Measurement, Blood-pressure, Non-invasive |
| Applicant | PPG INDUSTRIES, INC. ONE CAMPUS DR. Pleasantville, NY 10570 |
| Contact | Steve Brody |
| Correspondent | Steve Brody PPG INDUSTRIES, INC. ONE CAMPUS DR. Pleasantville, NY 10570 |
| Product Code | DXN |
| CFR Regulation Number | 870.1130 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-12-22 |
| Decision Date | 1988-02-29 |