The following data is part of a premarket notification filed by Hewlett-packard Co. with the FDA for Sonos Imaging System (2000/2500 & 1000/1500).
| Device ID | K952540 |
| 510k Number | K952540 |
| Device Name: | SONOS IMAGING SYSTEM (2000/2500 & 1000/1500) |
| Classification | System, Imaging, Pulsed Echo, Ultrasonic |
| Applicant | HEWLETT-PACKARD CO. 3000 MINUTEMAN RD. Andover, MA 01810 -1099 |
| Contact | Paul M Schrader |
| Correspondent | Paul M Schrader HEWLETT-PACKARD CO. 3000 MINUTEMAN RD. Andover, MA 01810 -1099 |
| Product Code | IYO |
| CFR Regulation Number | 892.1560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-05-23 |
| Decision Date | 1996-03-11 |
| Summary: | summary |