Nasal Aspirator (NS 13)
FDA 510(k) clearance K241852 · decided 2024-12-31
Clearance details
- K-number
- K241852
- Device name
- Nasal Aspirator (NS 13)
- Applicant
- Avita Corporation
- Decision
- Substantially Equivalent
- Date received
- 2024-06-27
- Decision date
- 2024-12-31
- Days to decision
- 187 days
- Clearance type
- Traditional
- Product code
- BTA
- Device class
- 2
- Regulation number
- 878.4780
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- New Taipei City, TW
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Avita Corporation
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.