LD-I 75 AND LD-I 200— 510(k) K072551
Substantially EquivalentMeditech International, Inc.
FDA 510(k) clearance K072551 for LD-I 75 AND LD-I 200, Substantially Equivalent on 2008-04-02. Applicant: Meditech International, Inc..
Clearance details
- Applicant
- Meditech International, Inc.
- Product code
- Code NHN
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Stamford, CT, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.