The following data is part of a premarket notification filed by Honeywell Hommed, Llc with the FDA for Honeywell Hommed Central Station 4.0.
| Device ID | K072272 |
| 510k Number | K072272 |
| Device Name: | HONEYWELL HOMMED CENTRAL STATION 4.0 |
| Classification | System, Measurement, Blood-pressure, Non-invasive |
| Applicant | HONEYWELL HOMMED, LLC 3400 INTERTECH DR. SUITE 200 Brookfield, WI 53045 |
| Contact | Michael Leigh |
| Correspondent | Michael Leigh HONEYWELL HOMMED, LLC 3400 INTERTECH DR. SUITE 200 Brookfield, WI 53045 |
| Product Code | DXN |
| CFR Regulation Number | 870.1130 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-08-15 |
| Decision Date | 2007-09-07 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00817644020000 | K072272 | 000 |