The following data is part of a premarket notification filed by Hewlett-packard Co. with the FDA for Hewlett-packard Series Of Disposable Nibp Cuffs.
| Device ID | K901252 |
| 510k Number | K901252 |
| Device Name: | HEWLETT-PACKARD SERIES OF DISPOSABLE NIBP CUFFS |
| Classification | Blood Pressure Cuff |
| Applicant | HEWLETT-PACKARD CO. 3000 MINUTEMAN RD. Andover, MA 01810 -1085 |
| Contact | Donald A Guthrie |
| Correspondent | Donald A Guthrie HEWLETT-PACKARD CO. 3000 MINUTEMAN RD. Andover, MA 01810 -1085 |
| Product Code | DXQ |
| CFR Regulation Number | 870.1120 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-03-16 |
| Decision Date | 1990-07-31 |