The following data is part of a premarket notification filed by Honeywell, Inc. with the FDA for Apm Dispos. Blood Pressure Transducer.
| Device ID | K851888 |
| 510k Number | K851888 |
| Device Name: | APM DISPOS. BLOOD PRESSURE TRANSDUCER |
| Classification | Transducer, Blood-pressure, Extravascular |
| Applicant | HONEYWELL, INC. ONE CAMPUS DR. Pleasantville, NY 10570 |
| Contact | Martin Kutik |
| Correspondent | Martin Kutik HONEYWELL, INC. ONE CAMPUS DR. Pleasantville, NY 10570 |
| Product Code | DRS |
| CFR Regulation Number | 870.2850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-05-01 |
| Decision Date | 1985-08-06 |