The following data is part of a premarket notification filed by Ostar Meditech Corp. with the FDA for Blood Pressure Monitor With Spectrum/p2, X2, A2, And K7.
Device ID | K050680 |
510k Number | K050680 |
Device Name: | BLOOD PRESSURE MONITOR WITH SPECTRUM/P2, X2, A2, AND K7 |
Classification | System, Measurement, Blood-pressure, Non-invasive |
Applicant | OSTAR MEDITECH CORP. 5F, NO. 46-4, MIN-CHIUAN RD. SHING-TIEN CITY Taipei Hsien, TW 231 |
Contact | Steven Chang |
Correspondent | Steven Chang OSTAR MEDITECH CORP. 5F, NO. 46-4, MIN-CHIUAN RD. SHING-TIEN CITY Taipei Hsien, TW 231 |
Product Code | DXN |
CFR Regulation Number | 870.1130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-03-16 |
Decision Date | 2005-05-13 |
Summary: | summary |