The following data is part of a premarket notification filed by Hewlett-packard Co. with the FDA for Accustress Exercise Testing System.
| Device ID | K953127 |
| 510k Number | K953127 |
| Device Name: | ACCUSTRESS EXERCISE TESTING SYSTEM |
| Classification | Computer, Diagnostic, Programmable |
| Applicant | HEWLETT-PACKARD CO. 1700 SOUTH BAKER ST. Mcminnville, OR 97128 |
| Contact | Nancy Winn |
| Correspondent | Nancy Winn HEWLETT-PACKARD CO. 1700 SOUTH BAKER ST. Mcminnville, OR 97128 |
| Product Code | DQK |
| CFR Regulation Number | 870.1425 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-07-05 |
| Decision Date | 1996-02-29 |