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FDA 510(k)

Wearable Device, Wearable Package

K-Number: K191272 · 2019-07-12

Decision Date2019-07-12
Product CodeMSX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Wearable Device, Wearable Package is the device name listed in this FDA 510(k) record. The listed applicant is Current Health , Ltd.. It received FDA 510(k) clearance on 2019-07-12 under 510(k) number K191272. The device is classified under product code MSX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Wearable Device, Wearable Package?

Wearable Device, Wearable Package is a medical device that received FDA 510(k) clearance on 2019-07-12. The listed applicant is Current Health , Ltd.. The 510(k) number is K191272.

When did Wearable Device, Wearable Package receive FDA 510(k) clearance?

Wearable Device, Wearable Package received FDA 510(k) clearance on 2019-07-12, under 510(k) number K191272.

Who is the listed applicant for Wearable Device, Wearable Package?

The FDA 510(k) record lists Current Health , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Wearable Device, Wearable Package?

The FDA product code for Wearable Device, Wearable Package is MSX.

Other records listing Current Health , Ltd. 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: MSX)

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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