EVERSTICK A&O
K-Number: K051953 · 2006-03-21
Advertisement
Device Summary
Frequently Asked Questions
What is the EVERSTICK A&O?
EVERSTICK A&O is a medical device that received FDA 510(k) clearance on 2006-03-21. The listed applicant is Stick Tech , Ltd.. The 510(k) number is K051953.
When did EVERSTICK A&O receive FDA 510(k) clearance?
EVERSTICK A&O received FDA 510(k) clearance on 2006-03-21, under 510(k) number K051953.
Who is the listed applicant for EVERSTICK A&O?
The FDA 510(k) record lists Stick Tech , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EVERSTICK A&O?
The FDA product code for EVERSTICK A&O is DYW.
Related Clinical Trials
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.
Other records listing Stick Tech , 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: DYW)
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.
Advertisement