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FDA 510(k)

ART-Plan

K-Number: K202700 · 2021-01-14

ApplicantTherapanacea
Decision Date2021-01-14
Product CodeQKB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ART-Plan is a medical device manufactured by Therapanacea. It received FDA 510(k) clearance on 2021-01-14 under approval number K202700. The device is classified under product code QKB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ART-Plan?

ART-Plan is a medical device that received FDA 510(k) clearance on 2021-01-14. It is manufactured by Therapanacea. The 510(k) number is K202700.

When was ART-Plan approved by the FDA?

ART-Plan received FDA 510(k) clearance on 2021-01-14, under approval number K202700.

What company makes ART-Plan?

ART-Plan is manufactured by Therapanacea.

What is the FDA product code for ART-Plan?

The FDA product code for ART-Plan is QKB.

Other Devices by Therapanacea

K220813ART-PLAN K232479ART-Plan

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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.

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