The following data is part of a premarket notification filed by Hewlett-packard Co. with the FDA for Model M1251a Mon. Full Disclosure Review System.
| Device ID | K905788 |
| 510k Number | K905788 |
| Device Name: | MODEL M1251A MON. FULL DISCLOSURE REVIEW SYSTEM |
| Classification | Display, Cathode-ray Tube, Medical |
| Applicant | HEWLETT-PACKARD CO. 175 WALTHAM ST. P.O.BOX 9030 Waltham, MA 02254 |
| Contact | Richard Beebe |
| Correspondent | Richard Beebe HEWLETT-PACKARD CO. 175 WALTHAM ST. P.O.BOX 9030 Waltham, MA 02254 |
| Product Code | DXJ |
| CFR Regulation Number | 870.2450 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-12-27 |
| Decision Date | 1991-06-06 |