The following data is part of a premarket notification filed by Lidco Ltd. with the FDA for Lidcoplus Hemodynamic Monitor System, Model Hm 70.
| Device ID | K023960 |
| 510k Number | K023960 |
| Device Name: | LIDCOPLUS HEMODYNAMIC MONITOR SYSTEM, MODEL HM 70 |
| Classification | Computer, Diagnostic, Pre-programmed, Single-function |
| Applicant | LIDCO LTD. 16 ORSMAN RD. London, GB N15qj |
| Contact | Gregory Speller |
| Correspondent | Gregory Speller LIDCO LTD. 16 ORSMAN RD. London, GB N15qj |
| Product Code | DXG |
| CFR Regulation Number | 870.1435 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-11-29 |
| Decision Date | 2003-01-09 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 05060110522507 | K023960 | 000 |
| 05060110520671 | K023960 | 000 |
| 05060110520664 | K023960 | 000 |
| 05060110520657 | K023960 | 000 |
| 05060110520640 | K023960 | 000 |
| 05060110520633 | K023960 | 000 |
| 05060110520626 | K023960 | 000 |
| 05060110520619 | K023960 | 000 |
| 05060110520602 | K023960 | 000 |
| 05060110520596 | K023960 | 000 |
| 05060110520589 | K023960 | 000 |
| 05060110520572 | K023960 | 000 |
| 05060110520565 | K023960 | 000 |
| 05060110520312 | K023960 | 000 |
| 05060110520275 | K023960 | 000 |
| 15060110520258 | K023960 | 000 |
| 05060110520688 | K023960 | 000 |
| 05060110520695 | K023960 | 000 |
| 05060110520701 | K023960 | 000 |
| 05060110522088 | K023960 | 000 |
| 15060110521804 | K023960 | 000 |
| 05060110521593 | K023960 | 000 |
| 05060110521340 | K023960 | 000 |
| 05060110521296 | K023960 | 000 |
| 05060110520978 | K023960 | 000 |
| 05060110520916 | K023960 | 000 |
| 05060110520909 | K023960 | 000 |
| 05060110520862 | K023960 | 000 |
| 05060110520855 | K023960 | 000 |
| 05060110520817 | K023960 | 000 |
| 05060110520800 | K023960 | 000 |
| 05060110520770 | K023960 | 000 |
| 05060110520725 | K023960 | 000 |
| 05060110520718 | K023960 | 000 |
| 15060110520104 | K023960 | 000 |