The following data is part of a premarket notification filed by Hewlett-packard Co. with the FDA for Hp Anesthesia Gas Monitor (watertrap), Model A02.
| Device ID | K982619 |
| 510k Number | K982619 |
| Device Name: | HP ANESTHESIA GAS MONITOR (WATERTRAP), MODEL A02 |
| Classification | Analyzer, Gas, Oxygen, Gaseous-phase |
| Applicant | HEWLETT-PACKARD CO. 3000 MINUTEMAN RD. Andover, MA 01810 -1085 |
| Contact | Elisabeth M George |
| Correspondent | Elisabeth M George HEWLETT-PACKARD CO. 3000 MINUTEMAN RD. Andover, MA 01810 -1085 |
| Product Code | CCL |
| CFR Regulation Number | 868.1720 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-07-27 |
| Decision Date | 1998-08-12 |
| Summary: | summary |