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FDA 510(k)

VORTRAN APM-Plus

K-Number: K182292 · 2019-09-18

Decision Date2019-09-18
Product CodeCAP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VORTRAN APM-Plus is the device name listed in this FDA 510(k) record. The listed applicant is Vortran Medical Technology 1, Inc.. It received FDA 510(k) clearance on 2019-09-18 under 510(k) 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. The listed applicant is Vortran Medical Technology 1, Inc.. The 510(k) number is K182292.

When did VORTRAN APM-Plus receive FDA 510(k) clearance?

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

Who is the listed applicant for VORTRAN APM-Plus?

The FDA 510(k) record lists Vortran Medical Technology 1, Inc. as the applicant. This does not by itself establish the device manufacturer.

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

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

Other records listing Vortran Medical Technology 1, Inc. 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: CAP)

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

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