INTERMITTENT PNEUMATIC COMPRESSION DEVICE— 510(k) K123830
Substantially EquivalentDalian Labtek Science & Development Co., Ltd.
FDA 510(k) clearance K123830 for INTERMITTENT PNEUMATIC COMPRESSION DEVICE, Substantially Equivalent on 2013-08-16. Applicant: Dalian Labtek Science & Development Co., Ltd..
Clearance details
- Applicant
- Dalian Labtek Science & Development Co., Ltd.
- Product code
- Code JOW
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shanghai, CN
Data sourced from openFDA. This site is unofficial and independent of the FDA.