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FDA 510(k)

CorVision® (91-205-Z0014)

K-Number: K260051 · 2026-05-12

ApplicantCorVent® Medical, Inc.
Decision Date2026-05-12
Product CodeMOD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CorVision® (91-205-Z0014) is a medical device manufactured by CorVent® Medical, Inc.. It received FDA 510(k) clearance on 2026-05-12 under approval number K260051. The device is classified under product code MOD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CorVision® (91-205-Z0014)?

CorVision® (91-205-Z0014) is a medical device that received FDA 510(k) clearance on 2026-05-12. It is manufactured by CorVent® Medical, Inc.. The 510(k) number is K260051.

When was CorVision® (91-205-Z0014) approved by the FDA?

CorVision® (91-205-Z0014) received FDA 510(k) clearance on 2026-05-12, under approval number K260051.

What company makes CorVision® (91-205-Z0014)?

CorVision® (91-205-Z0014) is manufactured by CorVent® Medical, Inc..

What is the FDA product code for CorVision® (91-205-Z0014)?

The FDA product code for CorVision® (91-205-Z0014) is MOD.

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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