The following data is part of a premarket notification filed by Healthstats International Pte. Ltd. with the FDA for A-pulse Caspro Model T7100, A-pulse Caspal Model T7200.
Device ID | K101002 |
510k Number | K101002 |
Device Name: | A-PULSE CASPRO MODEL T7100, A-PULSE CASPAL MODEL T7200 |
Classification | System, Measurement, Blood-pressure, Non-invasive |
Applicant | HEALTHSTATS INTERNATIONAL PTE. LTD. S65 W35739 PIPER ROAD Eagle, WI 53119 |
Contact | Stephen Gorski |
Correspondent | Stephen Gorski HEALTHSTATS INTERNATIONAL PTE. LTD. S65 W35739 PIPER ROAD Eagle, WI 53119 |
Product Code | DXN |
CFR Regulation Number | 870.1130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-04-12 |
Decision Date | 2010-06-08 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
08885014410050 | K101002 | 000 |
08885014410043 | K101002 | 000 |