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 |