The following data is part of a premarket notification filed by Hewlett-packard Co. with the FDA for Portable Patient Monitor.
| Device ID | K922974 |
| 510k Number | K922974 |
| Device Name: | PORTABLE PATIENT MONITOR |
| Classification | Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms) |
| Applicant | HEWLETT-PACKARD CO. 175 WYMAN ST. P.O. BOX 9030 Waltham, MS 02254 |
| Contact | David Osborn |
| Correspondent | David Osborn HEWLETT-PACKARD CO. 175 WYMAN ST. P.O. BOX 9030 Waltham, MS 02254 |
| Product Code | MHX |
| CFR Regulation Number | 870.1025 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-06-22 |
| Decision Date | 1992-12-07 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00884838011717 | K922974 | 000 |