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.. Device class: 2.
Clearance details
- Applicant
- Meditech International, Inc.
- Product code
- Code NHN
- Device class
- Class 2
- Regulation
- 21 CFR 890.5500
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Stamford, CT, US
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