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FDA 510(k)

Capillus 112, Capillus 244

K-Number: K192012 · 2019-09-12

ApplicantCapillus
Decision Date2019-09-12
Product CodeOAP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Capillus 112, Capillus 244 is a medical device manufactured by Capillus. It received FDA 510(k) clearance on 2019-09-12 under approval number K192012. The device is classified under product code OAP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Capillus 112, Capillus 244?

Capillus 112, Capillus 244 is a medical device that received FDA 510(k) clearance on 2019-09-12. It is manufactured by Capillus. The 510(k) number is K192012.

When was Capillus 112, Capillus 244 approved by the FDA?

Capillus 112, Capillus 244 received FDA 510(k) clearance on 2019-09-12, under approval number K192012.

What company makes Capillus 112, Capillus 244?

Capillus 112, Capillus 244 is manufactured by Capillus.

What is the FDA product code for Capillus 112, Capillus 244?

The FDA product code for Capillus 112, Capillus 244 is OAP.

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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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