Community Containers (Flap and Daisy)
FDA 510(k) clearance K252637 · decided 2025-10-14
Clearance details
- K-number
- K252637
- Device name
- Community Containers (Flap and Daisy)
- Applicant
- Keter Canada, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2025-08-20
- Decision date
- 2025-10-14
- Days to decision
- 55 days
- Clearance type
- Traditional
- Product code
- MMK
- Device class
- 2
- Regulation number
- 880.5570
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Milton, CA
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.