The following data is part of a premarket notification filed by Hewlett-packard Co. with the FDA for Hewlett-packard M2475b With 12-lead Option (#c90) Codemaster 100 Conitor/defibrillator.
| Device ID | K982025 |
| 510k Number | K982025 |
| Device Name: | HEWLETT-PACKARD M2475B WITH 12-LEAD OPTION (#C90) CODEMASTER 100 CONITOR/DEFIBRILLATOR |
| Classification | Automated External Defibrillators (non-wearable) |
| Applicant | HEWLETT-PACKARD CO. 3000 MINUTEMAN RD. Andover, MA 01810 -1085 |
| Contact | Richard J Petersen |
| Correspondent | Richard J Petersen HEWLETT-PACKARD CO. 3000 MINUTEMAN RD. Andover, MA 01810 -1085 |
| Product Code | MKJ |
| CFR Regulation Number | 870.5310 [🔎] |
| Decision | Se Subject To Tracking Reg (ST) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-06-09 |
| Decision Date | 1998-09-04 |
| Summary: | summary |