Female Luer Lock Cap
FDA 510(k) clearance K200425 · decided 2020-10-29
Clearance details
- K-number
- K200425
- Device name
- Female Luer Lock Cap
- Applicant
- Medsafety Solutions, LLC
- Decision
- Substantially Equivalent
- Date received
- 2020-02-20
- Decision date
- 2020-10-29
- Days to decision
- 252 days
- Clearance type
- Traditional
- Product code
- FPA
- Device class
- 2
- Regulation number
- 880.5440
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Centennial, CO, US
- Third-party review
- Yes
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.