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 |