Guidewire Locking Device— 510(k) K220247
Substantially EquivalentMicro-Tech (Nanjing) Co., Ltd.
FDA 510(k) clearance K220247 for Guidewire Locking Device, Substantially Equivalent on 2022-03-29. Applicant: Micro-Tech (Nanjing) Co., Ltd..
Clearance details
- Applicant
- Micro-Tech (Nanjing) Co., Ltd.
- Product code
- Code ODC
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Nanjing, CN
Data sourced from openFDA. This site is unofficial and independent of the FDA.