Guidewire Locking Device— 510(k) K220247

Name: FDA 510(k) clearance K220247
Creator: U.S. Food and Drug Administration
Published: 2022-03-29

Substantially Equivalent

Micro-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.. Device class: 2.

Clearance details

Applicant: Micro-Tech (Nanjing) Co., Ltd.
Product code: Code ODC
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 2022-01-28
Decision date: 2022-03-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Nanjing, CN

Download summary PDF View on FDA.gov ↗

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