510(k) K220126
K220126 is an FDA 510(k) premarket notification submitted by Geon Corporation for the device "Geonic Nasal Aspirator, Geonic Nasal Cleaner". The FDA issued a decision of Substantially Equivalent on February 2, 2023. The device falls under product code BTA (Pump, Portable, Aspiration (Manual Or Powered)), a Class II device regulated under 21 CFR 878.4780. Geon Corporation has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 2, 2023
- Date Received
- January 18, 2022
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Pump, Portable, Aspiration (Manual Or Powered)
- Device Class
- Class II
- Regulation Number
- 878.4780
- Review Panel
- SU
- Submission Type