ART-PLAN
K-Number: K220813 · 2022-06-17
Device Summary
Frequently Asked Questions
What is the ART-PLAN?
ART-PLAN is a medical device that received FDA 510(k) clearance on 2022-06-17. The listed applicant is Therapanacea. The 510(k) number is K220813.
When did ART-PLAN receive FDA 510(k) clearance?
ART-PLAN received FDA 510(k) clearance on 2022-06-17, under 510(k) number K220813.
Who is the listed applicant for ART-PLAN?
The FDA 510(k) record lists Therapanacea as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ART-PLAN?
The FDA product code for ART-PLAN is QKB.
Other records listing Therapanacea 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: QKB)
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.