The following data is part of a premarket notification filed by Cardicare Company, Ltd. with the FDA for Aneroid Sphygmomanometer With Stethoscope Model Hbpk-a.
Device ID | K082542 |
510k Number | K082542 |
Device Name: | ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE MODEL HBPK-A |
Classification | Blood Pressure Cuff |
Applicant | CARDICARE COMPANY, LTD. 9 YAN AN ROAD, WU SHAN PLAZA TOWN, UNIT 7003 Hangzhou, Zhejiang, CN 310002 |
Correspondent | Mark Job REGULATORY TECHNOLOGY SERVICES, LLC 1000 Westgate Drive, Suite 510k Saint Paul, MN 55114 |
Product Code | DXQ |
CFR Regulation Number | 870.1120 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | Yes |
Combination Product | No |
Date Received | 2008-09-03 |
Decision Date | 2008-09-17 |