The following data is part of a premarket notification filed by Microlife Intellectual Property Gmbh with the FDA for Microlife Wrist Watch Blood Pressure Monitor.
| Device ID | K141083 |
| 510k Number | K141083 |
| Device Name: | MICROLIFE WRIST WATCH BLOOD PRESSURE MONITOR |
| Classification | System, Measurement, Blood-pressure, Non-invasive |
| Applicant | MICROLIFE INTELLECTUAL PROPERTY GMBH 55 NORTHERN BOULEVARD SUITE 200 Great Neck, NY 10021 |
| Contact | Susan D Goldstein-falk |
| Correspondent | Susan D Goldstein-falk MICROLIFE INTELLECTUAL PROPERTY GMBH 55 NORTHERN BOULEVARD SUITE 200 Great Neck, NY 10021 |
| Product Code | DXN |
| CFR Regulation Number | 870.1130 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-04-28 |
| Decision Date | 2014-08-22 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00634782576158 | K141083 | 000 |