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FDA 510(k)

VORTRAN APM-Plus

K-Number: K182292 · 2019-09-18

ApplicantVortran Medical Technology 1, Inc.
Decision Date2019-09-18
Product CodeCAP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VORTRAN APM-Plus is a medical device manufactured by Vortran Medical Technology 1, Inc.. It received FDA 510(k) clearance on 2019-09-18 under approval number K182292. The device is classified under product code CAP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VORTRAN APM-Plus?

VORTRAN APM-Plus is a medical device that received FDA 510(k) clearance on 2019-09-18. It is manufactured by Vortran Medical Technology 1, Inc.. The 510(k) number is K182292.

When was VORTRAN APM-Plus approved by the FDA?

VORTRAN APM-Plus received FDA 510(k) clearance on 2019-09-18, under approval number K182292.

What company makes VORTRAN APM-Plus?

VORTRAN APM-Plus is manufactured by Vortran Medical Technology 1, Inc..

What is the FDA product code for VORTRAN APM-Plus?

The FDA product code for VORTRAN APM-Plus is CAP.

Other Devices by Vortran Medical Technology 1, Inc.

K153733VORTRAN Manometer K162968VORTRAN GO2VENT K173914VORTRAN Cuff Inflator (VCI) K202219VORTRAN GO2VENT with PEEP Valve

Related Devices (Code: CAP)

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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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