LIQUIBAND DUAL, MODEL LBD 001
FDA 510(k) clearance K102076 · decided 2011-02-18
Clearance details
- K-number
- K102076
- Device name
- LIQUIBAND DUAL, MODEL LBD 001
- Applicant
- Medlogic Global Limited
- Decision
- Substantially Equivalent
- Date received
- 2010-07-26
- Decision date
- 2011-02-18
- Days to decision
- 207 days
- Clearance type
- Traditional
- Product code
- MPN
- Device class
- 2
- Regulation number
- 878.4010
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Plympton, Plymouth, Devon, GB
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.