As-Nd
As-Nd is a Class II device made by Cardicare Company Ltd, cleared under FDA 510(k) K082542 on 17 Sep 2008 and listed in FDA GUDID since 25 Sep 2019 (UDI-DI 06970366970078), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number06970366970078 | Date25 Sep 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK082542 | Date17 Sep 2008 | StatusActive |
Official records
- AccessGUDID record 06970366970078
- FDA 510(k) database K082542
Across registries
- FDA 510(k) K082542 decided 17 Sep 2008 Active
- FDA GUDID UDI-DI 06970366970078 listed 25 Sep 2019 Listed
Timeline
- Cleared FDA 510(k) K082542
- Listed FDA GUDID 06970366970078
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Generic name
- Aneroid manual sphygmomanometer
- Model / reference
- AS-ND
- Primary DI / UDI-DI
- 06970366970078
- 510(k) Number
- FDA product code
- DXQ
- GMDN term
- Aneroid manual sphygmomanometer
- Device class
- Class II
- Regulation number
- 870.1120
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code DXQ (Blood Pressure Cuff).
- Tempa-Kuff Single Pat Pre-Gaged Balanced Disp Cuff by Pymah Corp.
- KLOCK WATCH STYLE DIGITAL BLOOD PRESSURE MONITOR by Card Guard Scientific Survival, Ltd.
- DISPOSABLE BLOOD PRESSURE CUF by CAREMATE MEDICAL DEVICE CO., LTD
- ETHOX NEONATAL BLOOD PRESSURE CUFF-STERILE/DISPOS. by Ethox Corp.
- TECHNICUFF by Technicuff Corp.
- DEROYAL STERILE NEONATAL BLOOD PRESSURE CUFF by DEROYAL INDUSTRIES, INC.
- EMPIRE N BLOOD PRESSURE MANOMETERS by Rudolf Riester GmbH & Co. KG
- Disposable Blood Pressure Cuff by Shenzhen Vistar Medical Supplies Co., Ltd.
- CLEAN CUFF BLOOD PRESSURE CUFF LINER by Steridyne Corp.
- FREEMAN ACETABULAR CUP by Depuy, Inc.