LERADO, COSCO
FDA 510(k) clearance K050290 · decided 2005-02-18
Clearance details
- K-number
- K050290
- Device name
- LERADO, COSCO
- Applicant
- Lerado Oversea Ltd. Twn Branch (Bvi)
- Decision
- Substantially Equivalent
- Date received
- 2005-02-07
- Decision date
- 2005-02-18
- Days to decision
- 11 days
- Clearance type
- Traditional
- Product code
- IOR
- Device class
- 1
- Regulation number
- 890.3850
- Medical specialty
- Physical Medicine
- Advisory committee
- Physical Medicine
- Location
- Hsin-Chu City, TW
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.