Kahook Dual Blade Glide (KDB Glide)— 510(k) K220891
Substantially EquivalentNew World Medical, Inc.
FDA 510(k) clearance K220891 for Kahook Dual Blade Glide (KDB Glide), Substantially Equivalent on 2024-05-17. Applicant: New World Medical, Inc..
Clearance details
- Applicant
- New World Medical, Inc.
- Product code
- Code QUQ
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Rancho Cucamonga, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.