Locking device
K-Number: K202237 · 2020-12-23
Device Summary
Frequently Asked Questions
What is the Locking device?
Locking device is a medical device that received FDA 510(k) clearance on 2020-12-23. The listed applicant is Hangzhou AGS MedTech Co., Ltd.. The 510(k) number is K202237.
When did Locking device receive FDA 510(k) clearance?
Locking device received FDA 510(k) clearance on 2020-12-23, under 510(k) number K202237.
Who is the listed applicant for Locking device?
The FDA 510(k) record lists Hangzhou AGS MedTech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Locking device?
The FDA product code for Locking device is ODC.
Other records listing Hangzhou AGS MedTech Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: ODC)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.