LIQUIDBAND FLOW CONTROL
FDA 510(k) clearance K122446 · decided 2012-10-26
Clearance details
- K-number
- K122446
- Device name
- LIQUIDBAND FLOW CONTROL
- Applicant
- Advanced Medical Solutions (Plymouth), Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2012-08-10
- Decision date
- 2012-10-26
- Days to decision
- 77 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
- Plymouth, GB
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
| Record | Firm | Date |
|---|---|---|
| a. Skin Adhesive McKesson LiquiBand Exceed 0.4 mL Liquid Dome Applicator Tip 2-Octyl Cyano recall (Z-1788-2022) | Mckesson Medical-Surgical Inc. Corporate Office | 2022-09-26 |