The following data is part of a premarket notification filed by Rossmax International Ltd. with the FDA for Rossmax Automatic Wristwatch Blood Pressure Monitor, Model Z43.
Device ID | K993460 |
510k Number | K993460 |
Device Name: | ROSSMAX AUTOMATIC WRISTWATCH BLOOD PRESSURE MONITOR, MODEL Z43 |
Classification | System, Measurement, Blood-pressure, Non-invasive |
Applicant | ROSSMAX INTERNATIONAL LTD. 2F. NO. 8, ALLEY 20 LANE 106 SECTION 3, NAN KANG ROAD Taipei, TW |
Contact | Michael Yeh |
Correspondent | Michael Yeh ROSSMAX INTERNATIONAL LTD. 2F. NO. 8, ALLEY 20 LANE 106 SECTION 3, NAN KANG ROAD Taipei, TW |
Product Code | DXN |
CFR Regulation Number | 870.1130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-10-13 |
Decision Date | 2000-01-11 |