SEKURIT SHARPS COLLECTION CONTAINER
FDA 510(k) clearance K063722 · decided 2007-03-05
Clearance details
- K-number
- K063722
- Device name
- SEKURIT SHARPS COLLECTION CONTAINER
- Applicant
- Techen Safety, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2006-12-15
- Decision date
- 2007-03-05
- Days to decision
- 80 days
- Clearance type
- Traditional
- Product code
- MMK
- Device class
- 2
- Regulation number
- 880.5570
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Great Neck, NY, US
- Third-party review
- Yes
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Techen Safety
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
No recalls on record reference this clearance.