The following data is part of a premarket notification filed by A C Cossor & Son (surgical) Limited with the FDA for Greenlight 300.
| Device ID | K040410 |
| 510k Number | K040410 |
| Device Name: | GREENLIGHT 300 |
| Classification | System, Measurement, Blood-pressure, Non-invasive |
| Applicant | A C COSSOR & SON (SURGICAL) LIMITED VALE ROAD London, GB N4 1ps |
| Contact | A J Cossor |
| Correspondent | A J Cossor A C COSSOR & SON (SURGICAL) LIMITED VALE ROAD London, GB N4 1ps |
| Product Code | DXN |
| CFR Regulation Number | 870.1130 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-02-18 |
| Decision Date | 2004-05-05 |